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rs794728897

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728897(A;A)
Make rs794728897(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38550994
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728897
ebirs794728897
HLIrs794728897
Exacrs794728897
Varsomers794728897
Maprs794728897
PheGenIrs794728897
hapmaprs794728897
1000 genomesrs794728897
hgdprs794728897
ensemblrs794728897
gopubmedrs794728897
geneviewrs794728897
scholarrs794728897
googlers794728897
pharmgkbrs794728897
gwascentralrs794728897
openSNPrs794728897
23andMers794728897
23andMe allrs794728897
SNP Nexus

SNPshotrs794728897
SNPdbers794728897
MSV3drs794728897
GWAS Ctlgrs794728897
Max Magnitude0
ClinVar
Risk rs794728897(A;A)
Alt rs794728897(A;A)
Reference rs794728897(T;T)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene SCN5A
CLNDBN not provided not specified
Reversed 1
HGVS NC_000003.11:g.38592485A>T
CLNSRC
CLNACC RCV000183120.1, RCV000223759.1,