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Gene
GRIN2B
GRIN2B is a gene. This site has 143 published variants inside it and 3 near it, each from a published genetic study, joining it to 5 condition pages.
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Reads by AI crawlers
Claude 0 ChatGPT 0 Google · Gemini 0 Perplexity 0 Meta AI 0 Microsoft · Copilot 2 Amazon 0 Apple 0 China (ByteDance, Huawei, Baidu…) 0 Others 1 Total 3 Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
Conditions it is linked to
Variants inside GRIN2B (143)
rs1805508 · Adventurousness rs1057518988 · Ataxia rs74442473 · Cerebrospinal AB1-42 levels in normal cognition rs1064796752 · Complex neurodevelopmental disorder rs1131691702 · Complex neurodevelopmental disorder rs1555112396 · Complex neurodevelopmental disorder rs1555133077 · Complex neurodevelopmental disorder rs1948651947 · Complex neurodevelopmental disorder rs1948686092 · Complex neurodevelopmental disorder rs1949419811 · Complex neurodevelopmental disorder rs1949425904 · Complex neurodevelopmental disorder rs886043237 · Complex neurodevelopmental disorder rs1060499659 · Developmental and epileptic encephalopathy, 27 rs1135401799 · Developmental and epileptic encephalopathy, 27 rs1555103172 · Developmental and epileptic encephalopathy, 27 rs1555112186 · Developmental and epileptic encephalopathy, 27 rs1591609136 · Developmental and epileptic encephalopathy, 27 rs1591638805 · Developmental and epileptic encephalopathy, 27 rs1948652423 · Developmental and epileptic encephalopathy, 27 rs1948653017 · Developmental and epileptic encephalopathy, 27 rs1949321492 · Developmental and epileptic encephalopathy, 27 rs2136413399 · Developmental and epileptic encephalopathy, 27 rs2497476034 · Developmental and epileptic encephalopathy, 27 rs2497597907 · Developmental and epileptic encephalopathy, 27 rs672601376 · Developmental and epileptic encephalopathy, 27 rs672601377 · Developmental and epileptic encephalopathy, 27 rs796052571 · Developmental and epileptic encephalopathy, 27 rs879253931 · Developmental and epileptic encephalopathy, 27 rs2497590335 · Developmental disorder rs1019385 · Educational attainment rs73047488 · General risk tolerance (MTAG) rs2497482289 · Global developmental delay rs2497471018 · GRIN2B-related disorder rs1555102536 · Inborn genetic diseases rs1555103150 · Inborn genetic diseases rs1555112021 · Inborn genetic diseases rs2497471746 · Inborn genetic diseases rs2497599845 · Inborn genetic diseases rs797044849 · Inborn genetic diseases rs797044930 · Inborn genetic diseases rs1057519004 · intellectual deficiency rs876661219 · intellectual deficiency rs1085307547 · Intellectual disability rs1591612223 · Intellectual disability rs1950069464 · Intellectual disability rs2497598118 · Intellectual disability rs1057518700 · Intellectual disability, autosomal dominant 6 rs1057519611 · Intellectual disability, autosomal dominant 6 rs1057519612 · Intellectual disability, autosomal dominant 6 rs1064794979 · Intellectual disability, autosomal dominant 6 rs1168374610 · Intellectual disability, autosomal dominant 6 rs1201643405 · Intellectual disability, autosomal dominant 6 rs1407009840 · Intellectual disability, autosomal dominant 6 rs1555102548 · Intellectual disability, autosomal dominant 6 rs1555103165 · Intellectual disability, autosomal dominant 6 rs1555103652 · Intellectual disability, autosomal dominant 6 rs1555103959 · Intellectual disability, autosomal dominant 6 rs1555103971 · Intellectual disability, autosomal dominant 6 rs1555103986 · Intellectual disability, autosomal dominant 6 rs1555110818 · Intellectual disability, autosomal dominant 6 rs1555110843 · Intellectual disability, autosomal dominant 6 rs1555112064 · Intellectual disability, autosomal dominant 6 rs1555112356 · Intellectual disability, autosomal dominant 6 rs1555112376 · Intellectual disability, autosomal dominant 6 rs1555119408 · Intellectual disability, autosomal dominant 6 rs1555133111 · Intellectual disability, autosomal dominant 6 rs1555133154 · Intellectual disability, autosomal dominant 6 rs1591612279 · Intellectual disability, autosomal dominant 6 rs1591612317 · Intellectual disability, autosomal dominant 6 rs1591643530 · Intellectual disability, autosomal dominant 6 rs1863527228 · Intellectual disability, autosomal dominant 6 rs1948651813 · Intellectual disability, autosomal dominant 6 rs1948652117 · Intellectual disability, autosomal dominant 6 rs1948652687 · Intellectual disability, autosomal dominant 6 rs1948713322 · Intellectual disability, autosomal dominant 6 rs1949319877 · Intellectual disability, autosomal dominant 6 rs1949320223 · Intellectual disability, autosomal dominant 6 rs1949320812 · Intellectual disability, autosomal dominant 6 rs1949320966 · Intellectual disability, autosomal dominant 6 rs1949321461 · Intellectual disability, autosomal dominant 6 rs1949321538 · Intellectual disability, autosomal dominant 6 rs1949368766 · Intellectual disability, autosomal dominant 6 rs1949368959 · Intellectual disability, autosomal dominant 6 rs1949369220 · Intellectual disability, autosomal dominant 6 rs1949419853 · Intellectual disability, autosomal dominant 6 rs1949420397 · Intellectual disability, autosomal dominant 6 rs1949421055 · Intellectual disability, autosomal dominant 6 rs1949427787 · Intellectual disability, autosomal dominant 6 rs2136409732 · Intellectual disability, autosomal dominant 6 rs2136409777 · Intellectual disability, autosomal dominant 6 rs2136409921 · Intellectual disability, autosomal dominant 6 rs2136415648 · Intellectual disability, autosomal dominant 6 rs2136415741 · Intellectual disability, autosomal dominant 6 rs2136415828 · Intellectual disability, autosomal dominant 6 rs2136415913 · Intellectual disability, autosomal dominant 6 rs2136470302 · Intellectual disability, autosomal dominant 6 rs2136470472 · Intellectual disability, autosomal dominant 6 rs2136470509 · Intellectual disability, autosomal dominant 6 rs2136479365 · Intellectual disability, autosomal dominant 6 rs2136479389 · Intellectual disability, autosomal dominant 6 rs2136479935 · Intellectual disability, autosomal dominant 6 rs2136629609 · Intellectual disability, autosomal dominant 6 rs2497476072 · Intellectual disability, autosomal dominant 6 rs2497485773 · Intellectual disability, autosomal dominant 6 rs2497582852 · Intellectual disability, autosomal dominant 6 rs2497583126 · Intellectual disability, autosomal dominant 6 rs2497597834 · Intellectual disability, autosomal dominant 6 rs2497597935 · Intellectual disability, autosomal dominant 6 rs2497597954 · Intellectual disability, autosomal dominant 6 rs2497598211 · Intellectual disability, autosomal dominant 6 rs2497602512 · Intellectual disability, autosomal dominant 6 rs2497684798 · Intellectual disability, autosomal dominant 6 rs2497778295 · Intellectual disability, autosomal dominant 6 rs387906636 · Intellectual disability, autosomal dominant 6 rs397514555 · Intellectual disability, autosomal dominant 6 rs397514556 · Intellectual disability, autosomal dominant 6 rs398122824 · Intellectual disability, autosomal dominant 6 rs398122825 · Intellectual disability, autosomal dominant 6 rs527236034 · Intellectual disability, autosomal dominant 6 rs672601378 · Intellectual disability, autosomal dominant 6 rs747172511 · Intellectual disability, autosomal dominant 6 rs748075089 · Intellectual disability, autosomal dominant 6 rs771157135 · Intellectual disability, autosomal dominant 6 rs774592932 · Intellectual disability, autosomal dominant 6 rs864309560 · Intellectual disability, autosomal dominant 6 rs867553974 · Intellectual disability, autosomal dominant 6 rs869312868 · Intellectual disability, autosomal dominant 6 rs876661041 · Intellectual disability, autosomal dominant 6 rs876661055 · Intellectual disability, autosomal dominant 6 rs876661064 · Intellectual disability, autosomal dominant 6 rs876661076 · Intellectual disability, autosomal dominant 6 rs876661151 · Intellectual disability, autosomal dominant 6 rs876661167 · Intellectual disability, autosomal dominant 6 rs879254016 · Intellectual disability, autosomal dominant 6 rs886041095 · Intellectual disability, autosomal dominant 6 rs886041295 · Intellectual disability, autosomal dominant 6 rs992479287 · Intellectual disability, autosomal dominant 6 rs35028277 · Myopia rs4764039 · Pediatric dental caries (decayed, missing and filled teeth >5) rs138009610 · Self-reported math ability rs1805552 · Smoking initiation rs1030056 · Systolic blood pressure rs28621435 · Systolic blood pressure
Variants near GRIN2B (3)
Positions outside the gene, filed under it because it is the closest. A variant near a gene does not always act through it.
See GRIN2B with everything it connects to on the Gene Knowledge Graph , or as data at /api/v1/genes/GRIN2B .
Licensed CC BY-NC 4.0: free to read, share and adapt for non-commercial use, naming MyGeneLog™ and linking the exact page. Commercial use, including training or serving a commercial AI system, needs a licence — https://www.mygenelog.com/license
GRIN2B gene. MyGeneLog™. https://www.mygenelog.com/genes/GRIN2B
A gene page gathers published research; it is not a test result and not medical advice. If a gene matters to your health, talk to a doctor or a genetic counsellor.