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Gene
SCN4A
SCN4A is a gene. This site has 96 published variants inside it and 2 near it, each from a published genetic study, joining it to 3 condition pages.
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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 SCN4A (96)
rs1597978607 · Arthrogryposis multiplex congenita rs8074752 · Aspartate aminotransferase levels rs879253789 · Congenital myasthenic syndrome rs1598406692 · Congenital myasthenic syndrome 16 rs1908668408 · Congenital myasthenic syndrome 16 rs777998706 · Congenital myasthenic syndrome 16 rs2509290730 · Congenital myopathy 22A, classic rs2509318035 · Congenital myopathy 22A, classic rs2509284285 · Congenital myopathy 22B, severe fetal rs2509285379 · Congenital myopathy 22B, severe fetal rs2509289236 · Congenital myopathy 22B, severe fetal rs2509317969 · Congenital myopathy 22B, severe fetal rs4968680 · Forced expiratory volume (baseline) rs2109079 · Height (baseline) rs75828444 · Height (baseline) rs2877372 · Hip circumference adjusted for BMI rs1057521065 · Hyperkalemic periodic paralysis rs1064794243 · Hyperkalemic periodic paralysis rs1064795409 · Hyperkalemic periodic paralysis rs1199222144 · Hyperkalemic periodic paralysis rs1224997537 · Hyperkalemic periodic paralysis rs1331907655 · Hyperkalemic periodic paralysis rs1358028812 · Hyperkalemic periodic paralysis rs1555600605 · Hyperkalemic periodic paralysis rs1555601448 · Hyperkalemic periodic paralysis rs1555603671 · Hyperkalemic periodic paralysis rs1567816461 · Hyperkalemic periodic paralysis rs1567816549 · Hyperkalemic periodic paralysis rs1567817380 · Hyperkalemic periodic paralysis rs1597985462 · Hyperkalemic periodic paralysis rs1598405334 · Hyperkalemic periodic paralysis rs1908593639 · Hyperkalemic periodic paralysis rs1908594231 · Hyperkalemic periodic paralysis rs1909453191 · Hyperkalemic periodic paralysis rs1909519361 · Hyperkalemic periodic paralysis rs2144773878 · Hyperkalemic periodic paralysis rs2144798676 · Hyperkalemic periodic paralysis rs2144798704 · Hyperkalemic periodic paralysis rs2509287979 · Hyperkalemic periodic paralysis rs2509291040 · Hyperkalemic periodic paralysis rs2509308046 · Hyperkalemic periodic paralysis rs2509313987 · Hyperkalemic periodic paralysis rs2509315709 · Hyperkalemic periodic paralysis rs557322255 · Hyperkalemic periodic paralysis rs749400108 · Hyperkalemic periodic paralysis rs759347899 · Hyperkalemic periodic paralysis rs763893717 · Hyperkalemic periodic paralysis rs771340029 · Hyperkalemic periodic paralysis rs774453167 · Hyperkalemic periodic paralysis rs775244273 · Hyperkalemic periodic paralysis rs780703403 · Hyperkalemic periodic paralysis rs80338955 · Hyperkalemic periodic paralysis rs80338957 · Hyperkalemic periodic paralysis rs80338959 · Hyperkalemic periodic paralysis rs80338960 · Hyperkalemic periodic paralysis rs80338962 · Hyperkalemic periodic paralysis rs864622785 · Hyperkalemic periodic paralysis rs865887222 · Hyperkalemic periodic paralysis rs886041805 · Hyperkalemic periodic paralysis rs943370469 · Hyperkalemic periodic paralysis rs121908555 · Hypokalemic periodic paralysis, type 2 rs1287863349 · Hypokalemic periodic paralysis, type 2 rs2144774834 · Hypokalemic periodic paralysis, type 2 rs527236148 · Hypokalemic periodic paralysis, type 2 rs527236150 · Hypokalemic periodic paralysis, type 2 rs80338784 · Hypokalemic periodic paralysis, type 2 rs80338785 · Hypokalemic periodic paralysis, type 2 rs80338788 · Hypokalemic periodic paralysis, type 2 rs80338789 · Hypokalemic periodic paralysis, type 2 rs867587467 · Inborn genetic diseases rs121908549 · Myotonia congenita, atypical, acetazolamide-responsive rs121908556 · Normokalemic periodic paralysis, potassium-sensitive rs121908557 · Normokalemic periodic paralysis, potassium-sensitive rs121908544 · Paramyotonia congenita of Von Eulenburg rs121908545 · Paramyotonia congenita of Von Eulenburg rs121908547 · Paramyotonia congenita of Von Eulenburg rs121908550 · Paramyotonia congenita of Von Eulenburg rs121908551 · Paramyotonia congenita of Von Eulenburg rs121908554 · Paramyotonia congenita of Von Eulenburg rs121908559 · Paramyotonia congenita of Von Eulenburg rs121908561 · Paramyotonia congenita of Von Eulenburg rs2144793242 · Paramyotonia congenita of Von Eulenburg rs2509285181 · Paramyotonia congenita of Von Eulenburg rs80338792 · Paramyotonia congenita of Von Eulenburg rs80338956 · Paramyotonia congenita of Von Eulenburg rs121908560 · Paramyotonia congenita/hyperkalemic periodic paralysis rs121908546 · Paramyotonia congenita/myotonia congenita rs121908548 · Potassium-aggravated myotonia rs121908552 · Potassium-aggravated myotonia rs2509291006 · Potassium-aggravated myotonia rs914586984 · Potassium-aggravated myotonia rs1210934866 · SCN4A-related disorder rs2509305424 · SCN4A-related disorder rs2509325722 · SCN4A-related disorder rs1908691206 · SCN4A-related non-dystrophic myotonia rs2144779553 · SCN4A-related non-dystrophic myotonia
Variants near SCN4A (2)
Positions outside the gene, filed under it because it is the closest. A variant near a gene does not always act through it.
See SCN4A with everything it connects to on the Gene Knowledge Graph , or as data at /api/v1/genes/SCN4A .
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SCN4A gene. MyGeneLog™. https://www.mygenelog.com/genes/SCN4A
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.