ClinVar Miner

List of variants in gene SEPTIN9 reported as benign for amyotrophic neuralgia

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
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HGVS dbSNP
NM_001113491.2(SEPTIN9):c.1726A>G (p.Met576Val) rs2627223
NM_001113491.2(SEPTIN9):c.721+2405G>A rs2164449
NM_001113491.2(SEPTIN9):c.76+19T>C rs4789439
NM_001113491.2(SEPTIN9):c.77-28563T>C rs7217986

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