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rs796052964

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052964(C;T)
Make rs796052964(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166051841
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796052964
ebirs796052964
HLIrs796052964
Exacrs796052964
Varsomers796052964
Maprs796052964
PheGenIrs796052964
hapmaprs796052964
1000 genomesrs796052964
hgdprs796052964
ensemblrs796052964
gopubmedrs796052964
geneviewrs796052964
scholarrs796052964
googlers796052964
pharmgkbrs796052964
gwascentralrs796052964
openSNPrs796052964
23andMers796052964
23andMe allrs796052964
SNP Nexus

SNPshotrs796052964
SNPdbers796052964
MSV3drs796052964
GWAS Ctlgrs796052964
Max Magnitude0
ClinVar
Risk rs796052964(T;T)
Alt rs796052964(T;T)
Reference rs796052964(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166908351G>A
CLNSRC
CLNACC RCV000188849.1,