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rs796052981

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052981(C;C)
Make rs796052981(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166039508
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796052981
ebirs796052981
HLIrs796052981
Exacrs796052981
Varsomers796052981
Maprs796052981
PheGenIrs796052981
hapmaprs796052981
1000 genomesrs796052981
hgdprs796052981
ensemblrs796052981
gopubmedrs796052981
geneviewrs796052981
scholarrs796052981
googlers796052981
pharmgkbrs796052981
gwascentralrs796052981
openSNPrs796052981
23andMers796052981
23andMe allrs796052981
SNP Nexus

SNPshotrs796052981
SNPdbers796052981
MSV3drs796052981
GWAS Ctlgrs796052981
Max Magnitude0
ClinVar
Risk rs796052981(C;C)
Alt rs796052981(C;C)
Reference rs796052981(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166896018A>G
CLNSRC
CLNACC RCV000188890.1,