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rs794728877

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728877(C;T)
Make rs794728877(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38560398
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728877
ebirs794728877
HLIrs794728877
Exacrs794728877
Varsomers794728877
Maprs794728877
PheGenIrs794728877
hapmaprs794728877
1000 genomesrs794728877
hgdprs794728877
ensemblrs794728877
gopubmedrs794728877
geneviewrs794728877
scholarrs794728877
googlers794728877
pharmgkbrs794728877
gwascentralrs794728877
openSNPrs794728877
23andMers794728877
23andMe allrs794728877
SNP Nexus

SNPshotrs794728877
SNPdbers794728877
MSV3drs794728877
GWAS Ctlgrs794728877
Max Magnitude0
ClinVar
Risk rs794728877(T;T)
Alt rs794728877(T;T)
Reference rs794728877(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38601889G>A
CLNSRC
CLNACC RCV000183054.1,