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rs796052962

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052962(A;A)
Make rs796052962(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166051935
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796052962
ebirs796052962
HLIrs796052962
Exacrs796052962
Varsomers796052962
Maprs796052962
PheGenIrs796052962
hapmaprs796052962
1000 genomesrs796052962
hgdprs796052962
ensemblrs796052962
gopubmedrs796052962
geneviewrs796052962
scholarrs796052962
googlers796052962
pharmgkbrs796052962
gwascentralrs796052962
openSNPrs796052962
23andMers796052962
23andMe allrs796052962
SNP Nexus

SNPshotrs796052962
SNPdbers796052962
MSV3drs796052962
GWAS Ctlgrs796052962
Max Magnitude0
ClinVar
Risk rs796052962(A;A)
Alt rs796052962(A;A)
Reference rs796052962(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166908445C>T
CLNSRC
CLNACC RCV000188844.2,