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rs794728857

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728857(A;A)
Make rs794728857(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38604084
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728857
ebirs794728857
HLIrs794728857
Exacrs794728857
Varsomers794728857
Maprs794728857
PheGenIrs794728857
hapmaprs794728857
1000 genomesrs794728857
hgdprs794728857
ensemblrs794728857
gopubmedrs794728857
geneviewrs794728857
scholarrs794728857
googlers794728857
pharmgkbrs794728857
gwascentralrs794728857
openSNPrs794728857
23andMers794728857
23andMe allrs794728857
SNP Nexus

SNPshotrs794728857
SNPdbers794728857
MSV3drs794728857
GWAS Ctlgrs794728857
Max Magnitude0
ClinVar
Risk rs794728857(A;A)
Alt rs794728857(A;A)
Reference rs794728857(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38645575C>T
CLNSRC
CLNACC RCV000182974.1,