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rs796052972

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052972(A;A)
Make rs796052972(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166047644
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796052972
ebirs796052972
HLIrs796052972
Exacrs796052972
Varsomers796052972
Maprs796052972
PheGenIrs796052972
hapmaprs796052972
1000 genomesrs796052972
hgdprs796052972
ensemblrs796052972
gopubmedrs796052972
geneviewrs796052972
scholarrs796052972
googlers796052972
pharmgkbrs796052972
gwascentralrs796052972
openSNPrs796052972
23andMers796052972
23andMe allrs796052972
SNP Nexus

SNPshotrs796052972
SNPdbers796052972
MSV3drs796052972
GWAS Ctlgrs796052972
Max Magnitude0
ClinVar
Risk rs796052972(A;A)
Alt rs796052972(A;A)
Reference rs796052972(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166904154C>T
CLNSRC
CLNACC RCV000188862.1,