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rs763400390

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs763400390(C;T)
Make rs763400390(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position166041470
GeneSCN1A
is asnp
is mentioned by
dbSNPrs763400390
ebirs763400390
HLIrs763400390
Exacrs763400390
Varsomers763400390
Maprs763400390
PheGenIrs763400390
hapmaprs763400390
1000 genomesrs763400390
hgdprs763400390
ensemblrs763400390
gopubmedrs763400390
geneviewrs763400390
scholarrs763400390
googlers763400390
pharmgkbrs763400390
gwascentralrs763400390
openSNPrs763400390
23andMers763400390
23andMe allrs763400390
SNP Nexus

SNPshotrs763400390
SNPdbers763400390
MSV3drs763400390
GWAS Ctlgrs763400390
Max Magnitude0
ClinVar
Risk rs763400390(A,T;A,T)
Alt rs763400390(A,T;A,T)
Reference rs763400390(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166897980C>A
CLNSRC
CLNACC RCV000189081.2,