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rs796052953

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052953(A;A)
Make rs796052953(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166058689
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796052953
ebirs796052953
HLIrs796052953
Exacrs796052953
Varsomers796052953
Maprs796052953
PheGenIrs796052953
hapmaprs796052953
1000 genomesrs796052953
hgdprs796052953
ensemblrs796052953
gopubmedrs796052953
geneviewrs796052953
scholarrs796052953
googlers796052953
pharmgkbrs796052953
gwascentralrs796052953
openSNPrs796052953
23andMers796052953
23andMe allrs796052953
SNP Nexus

SNPshotrs796052953
SNPdbers796052953
MSV3drs796052953
GWAS Ctlgrs796052953
Max Magnitude0
ClinVar
Risk rs796052953(A;A)
Alt rs796052953(A;A)
Reference rs796052953(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166915199C>T
CLNSRC
CLNACC RCV000188826.2,