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rs794728871

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728871(C;T)
Make rs794728871(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38581098
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728871
ebirs794728871
HLIrs794728871
Exacrs794728871
Varsomers794728871
Maprs794728871
PheGenIrs794728871
hapmaprs794728871
1000 genomesrs794728871
hgdprs794728871
ensemblrs794728871
gopubmedrs794728871
geneviewrs794728871
scholarrs794728871
googlers794728871
pharmgkbrs794728871
gwascentralrs794728871
openSNPrs794728871
23andMers794728871
23andMe allrs794728871
SNP Nexus

SNPshotrs794728871
SNPdbers794728871
MSV3drs794728871
GWAS Ctlgrs794728871
Max Magnitude0
ClinVar
Risk rs794728871(T;T)
Alt rs794728871(T;T)
Reference rs794728871(C;C)
Significance Pathogenic
Disease not specified
Variation info
Gene SCN5A
CLNDBN not specified
Reversed 1
HGVS NC_000003.11:g.38622589G>A
CLNSRC
CLNACC RCV000183017.3,