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rs796052974

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052974(G;G)
Make rs796052974(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166046952
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796052974
ebirs796052974
HLIrs796052974
Exacrs796052974
Varsomers796052974
Maprs796052974
PheGenIrs796052974
hapmaprs796052974
1000 genomesrs796052974
hgdprs796052974
ensemblrs796052974
gopubmedrs796052974
geneviewrs796052974
scholarrs796052974
googlers796052974
pharmgkbrs796052974
gwascentralrs796052974
openSNPrs796052974
23andMers796052974
23andMe allrs796052974
SNP Nexus

SNPshotrs796052974
SNPdbers796052974
MSV3drs796052974
GWAS Ctlgrs796052974
Max Magnitude0
ClinVar
Risk rs796052974(G;G)
Alt rs796052974(G;G)
Reference rs796052974(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166903462A>C
CLNSRC
CLNACC RCV000188866.2,