Have questions? Visit https://www.reddit.com/r/SNPedia

rs121908921

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908921(A;A)
Make rs121908921(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position166306531
GeneSCN9A
is asnp
is mentioned by
dbSNPrs121908921
ebirs121908921
HLIrs121908921
Exacrs121908921
Varsomers121908921
Maprs121908921
PheGenIrs121908921
hapmaprs121908921
1000 genomesrs121908921
hgdprs121908921
ensemblrs121908921
gopubmedrs121908921
geneviewrs121908921
scholarrs121908921
googlers121908921
pharmgkbrs121908921
gwascentralrs121908921
openSNPrs121908921
23andMers121908921
23andMe allrs121908921
SNP Nexus

SNPshotrs121908921
SNPdbers121908921
MSV3drs121908921
GWAS Ctlgrs121908921
Max Magnitude0
OMIM603415
Desc
Variant0021
Relatedalso
ClinVar
Risk rs121908921(A,T;A,T)
Alt rs121908921(A,T;A,T)
Reference rs121908921(C;C)
Significance Pathogenic
Disease Febrile seizures
Variation info
Gene SCN9A
CLNDBN Febrile seizures, familial, 3b
Reversed 1
HGVS NC_000002.11:g.167163041G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006741.3,