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rs794728933

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728933(A;A)
Make rs794728933(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38566404
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728933
ebirs794728933
HLIrs794728933
Exacrs794728933
Varsomers794728933
Maprs794728933
PheGenIrs794728933
hapmaprs794728933
1000 genomesrs794728933
hgdprs794728933
ensemblrs794728933
gopubmedrs794728933
geneviewrs794728933
scholarrs794728933
googlers794728933
pharmgkbrs794728933
gwascentralrs794728933
openSNPrs794728933
23andMers794728933
23andMe allrs794728933
SNP Nexus

SNPshotrs794728933
SNPdbers794728933
MSV3drs794728933
GWAS Ctlgrs794728933
Max Magnitude0
ClinVar
Risk rs794728933(A;A)
Alt rs794728933(A;A)
Reference rs794728933(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38607895C>T
CLNSRC
CLNACC RCV000183186.1,