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Gene
GFM1
GFM1 is a gene. This site has 47 published variants inside it, each from a published genetic study, joining it to 1 condition page.
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Reads by AI crawlers
Claude 0 ChatGPT 0 Google · Gemini 0 Perplexity 0 Meta AI 0 Microsoft · Copilot 0 Amazon 0 Apple 0 China (ByteDance, Huawei, Baidu…) 0 Others 0 Total 0 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 GFM1 (47)
rs751069628 · Combined oxidative phosphorylation deficiency rs2303909 · Diastolic blood pressure rs8455 · Diastolic blood pressure rs184291369 · Eosinophil side scatter rs2473037328 · GFM1-related disorder rs2474011247 · GFM1-related disorder rs774456344 · GFM1-related disorder rs1560135491 · GFM1-related disorders rs1004779078 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs119470018 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs119470019 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs119470020 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs1262218849 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs1332636394 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs139430866 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs1402362655 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs1416173655 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs143031224 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs1449057162 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs1456835520 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs1462851267 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs1553847587 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs1576757241 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs1721865059 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs1725442904 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs200697129 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs201408725 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs2108051038 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs2108102423 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs2473064367 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs2473960497 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs2473961042 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs541171482 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs756718556 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs757524798 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs760266828 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs763344414 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs766234016 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs767325554 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs771890880 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs775919783 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs863224032 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs867885977 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs889180452 · Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 rs747437028 · Malignant tumor of urinary bladder rs760290078 · Malignant tumor of urinary bladder rs142350615 · Retinoic acid receptor responder protein 1 levels
See GFM1 with everything it connects to on the Gene Knowledge Graph , or as data at /api/v1/genes/GFM1 .
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
GFM1 gene. MyGeneLog™. https://www.mygenelog.com/genes/GFM1
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.