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rs796052961

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052961(C;C)
Make rs796052961(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166052884
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796052961
ebirs796052961
HLIrs796052961
Exacrs796052961
Varsomers796052961
Maprs796052961
PheGenIrs796052961
hapmaprs796052961
1000 genomesrs796052961
hgdprs796052961
ensemblrs796052961
gopubmedrs796052961
geneviewrs796052961
scholarrs796052961
googlers796052961
pharmgkbrs796052961
gwascentralrs796052961
openSNPrs796052961
23andMers796052961
23andMe allrs796052961
SNP Nexus

SNPshotrs796052961
SNPdbers796052961
MSV3drs796052961
GWAS Ctlgrs796052961
Max Magnitude0
ClinVar
Risk rs796052961(C;C)
Alt rs796052961(C;C)
Reference rs796052961(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166909394A>G
CLNSRC
CLNACC RCV000188840.2,