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rs796052976

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052976(C;T)
Make rs796052976(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166046799
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796052976
ebirs796052976
HLIrs796052976
Exacrs796052976
Varsomers796052976
Maprs796052976
PheGenIrs796052976
hapmaprs796052976
1000 genomesrs796052976
hgdprs796052976
ensemblrs796052976
gopubmedrs796052976
geneviewrs796052976
scholarrs796052976
googlers796052976
pharmgkbrs796052976
gwascentralrs796052976
openSNPrs796052976
23andMers796052976
23andMe allrs796052976
SNP Nexus

SNPshotrs796052976
SNPdbers796052976
MSV3drs796052976
GWAS Ctlgrs796052976
Max Magnitude0
ClinVar
Risk rs796052976(T;T)
Alt rs796052976(T;T)
Reference rs796052976(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166903309G>A
CLNSRC
CLNACC RCV000188869.1,