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rs794728929

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728929(C;T)
Make rs794728929(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38585996
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728929
ebirs794728929
HLIrs794728929
Exacrs794728929
Varsomers794728929
Maprs794728929
PheGenIrs794728929
hapmaprs794728929
1000 genomesrs794728929
hgdprs794728929
ensemblrs794728929
gopubmedrs794728929
geneviewrs794728929
scholarrs794728929
googlers794728929
pharmgkbrs794728929
gwascentralrs794728929
openSNPrs794728929
23andMers794728929
23andMe allrs794728929
SNP Nexus

SNPshotrs794728929
SNPdbers794728929
MSV3drs794728929
GWAS Ctlgrs794728929
Max Magnitude0
ClinVar
Risk rs794728929(T;T)
Alt rs794728929(T;T)
Reference rs794728929(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38627487G>A
CLNSRC
CLNACC RCV000183177.1,