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rs796052963

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052963(A;T)
Make rs796052963(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166051856
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796052963
ebirs796052963
HLIrs796052963
Exacrs796052963
Varsomers796052963
Maprs796052963
PheGenIrs796052963
hapmaprs796052963
1000 genomesrs796052963
hgdprs796052963
ensemblrs796052963
gopubmedrs796052963
geneviewrs796052963
scholarrs796052963
googlers796052963
pharmgkbrs796052963
gwascentralrs796052963
openSNPrs796052963
23andMers796052963
23andMe allrs796052963
SNP Nexus

SNPshotrs796052963
SNPdbers796052963
MSV3drs796052963
GWAS Ctlgrs796052963
Max Magnitude0
ClinVar
Risk rs796052963(T;T)
Alt rs796052963(T;T)
Reference rs796052963(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166908366T>A
CLNSRC
CLNACC RCV000188848.1,