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rs796052959

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052959(A;A)
Make rs796052959(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166052944
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796052959
ebirs796052959
HLIrs796052959
Exacrs796052959
Varsomers796052959
Maprs796052959
PheGenIrs796052959
hapmaprs796052959
1000 genomesrs796052959
hgdprs796052959
ensemblrs796052959
gopubmedrs796052959
geneviewrs796052959
scholarrs796052959
googlers796052959
pharmgkbrs796052959
gwascentralrs796052959
openSNPrs796052959
23andMers796052959
23andMe allrs796052959
SNP Nexus

SNPshotrs796052959
SNPdbers796052959
MSV3drs796052959
GWAS Ctlgrs796052959
Max Magnitude0
ClinVar
Risk rs796052959(A;A)
Alt rs796052959(A;A)
Reference rs796052959(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166909454C>T
CLNSRC
CLNACC RCV000188838.2,