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rs796053089

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053089(C;T)
Make rs796053089(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166058639
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053089
ebirs796053089
HLIrs796053089
Exacrs796053089
Varsomers796053089
Maprs796053089
PheGenIrs796053089
hapmaprs796053089
1000 genomesrs796053089
hgdprs796053089
ensemblrs796053089
gopubmedrs796053089
geneviewrs796053089
scholarrs796053089
googlers796053089
pharmgkbrs796053089
gwascentralrs796053089
openSNPrs796053089
23andMers796053089
23andMe allrs796053089
SNP Nexus

SNPshotrs796053089
SNPdbers796053089
MSV3drs796053089
GWAS Ctlgrs796053089
Max Magnitude0
ClinVar
Risk rs796053089(T;T)
Alt rs796053089(T;T)
Reference rs796053089(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166915149G>A
CLNSRC
CLNACC RCV000189071.1,