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rs121909673

From SNPedia

OMIM137164
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121909673(A;A)
Alt rs121909673(A;A)
Reference rs121909673(G;G)
Significance Other
Disease Epilepsy Familial febrile seizures 8 not provided
Variation info
Gene GABRG2
CLNDBN Epilepsy, childhood absence 2 Familial febrile seizures 8 not provided
Reversed 0
HGVS NC_000005.9:g.161520971G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017592.3, RCV000017593.28, RCV000187520.2,