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rs794728884

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728884(C;C)
Make rs794728884(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38556469
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728884
ebirs794728884
HLIrs794728884
Exacrs794728884
Varsomers794728884
Maprs794728884
PheGenIrs794728884
hapmaprs794728884
1000 genomesrs794728884
hgdprs794728884
ensemblrs794728884
gopubmedrs794728884
geneviewrs794728884
scholarrs794728884
googlers794728884
pharmgkbrs794728884
gwascentralrs794728884
openSNPrs794728884
23andMers794728884
23andMe allrs794728884
SNP Nexus

SNPshotrs794728884
SNPdbers794728884
MSV3drs794728884
GWAS Ctlgrs794728884
Max Magnitude0
ClinVar
Risk rs794728884(C;C)
Alt rs794728884(C;C)
Reference rs794728884(T;T)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene SCN5A
CLNDBN not specified
Reversed 1
HGVS NC_000003.11:g.38597960A>G
CLNSRC
CLNACC RCV000183075.2,