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rs781746113

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs781746113(C;T)
Make rs781746113(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position166048929
GeneSCN1A
is asnp
is mentioned by
dbSNPrs781746113
ebirs781746113
HLIrs781746113
Exacrs781746113
Varsomers781746113
Maprs781746113
PheGenIrs781746113
hapmaprs781746113
1000 genomesrs781746113
hgdprs781746113
ensemblrs781746113
gopubmedrs781746113
geneviewrs781746113
scholarrs781746113
googlers781746113
pharmgkbrs781746113
gwascentralrs781746113
openSNPrs781746113
23andMers781746113
23andMe allrs781746113
SNP Nexus

SNPshotrs781746113
SNPdbers781746113
MSV3drs781746113
GWAS Ctlgrs781746113
Max Magnitude0
ClinVar
Risk rs781746113(A,T;A,T)
Alt rs781746113(A,T;A,T)
Reference rs781746113(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166905439C>A
CLNSRC
CLNACC RCV000189077.1,