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rs796052971

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052971(C;T)
Make rs796052971(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166047685
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796052971
ebirs796052971
HLIrs796052971
Exacrs796052971
Varsomers796052971
Maprs796052971
PheGenIrs796052971
hapmaprs796052971
1000 genomesrs796052971
hgdprs796052971
ensemblrs796052971
gopubmedrs796052971
geneviewrs796052971
scholarrs796052971
googlers796052971
pharmgkbrs796052971
gwascentralrs796052971
openSNPrs796052971
23andMers796052971
23andMe allrs796052971
SNP Nexus

SNPshotrs796052971
SNPdbers796052971
MSV3drs796052971
GWAS Ctlgrs796052971
Max Magnitude0
ClinVar
Risk rs796052971(T;T)
Alt rs796052971(T;T)
Reference rs796052971(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166904195G>A
CLNSRC
CLNACC RCV000188860.2,