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rs794728858

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728858(A;A)
Make rs794728858(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38599051
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728858
ebirs794728858
HLIrs794728858
Exacrs794728858
Varsomers794728858
Maprs794728858
PheGenIrs794728858
hapmaprs794728858
1000 genomesrs794728858
hgdprs794728858
ensemblrs794728858
gopubmedrs794728858
geneviewrs794728858
scholarrs794728858
googlers794728858
pharmgkbrs794728858
gwascentralrs794728858
openSNPrs794728858
23andMers794728858
23andMe allrs794728858
SNP Nexus

SNPshotrs794728858
SNPdbers794728858
MSV3drs794728858
GWAS Ctlgrs794728858
Max Magnitude0
ClinVar
Risk rs794728858(A;A)
Alt rs794728858(A;A)
Reference rs794728858(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38640542C>T
CLNSRC
CLNACC RCV000182989.2,