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rs794728879

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728879(C;C)
Make rs794728879(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38560146
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728879
ebirs794728879
HLIrs794728879
Exacrs794728879
Varsomers794728879
Maprs794728879
PheGenIrs794728879
hapmaprs794728879
1000 genomesrs794728879
hgdprs794728879
ensemblrs794728879
gopubmedrs794728879
geneviewrs794728879
scholarrs794728879
googlers794728879
pharmgkbrs794728879
gwascentralrs794728879
openSNPrs794728879
23andMers794728879
23andMe allrs794728879
SNP Nexus

SNPshotrs794728879
SNPdbers794728879
MSV3drs794728879
GWAS Ctlgrs794728879
Max Magnitude0
ClinVar
Risk rs794728879(C,T;C,T)
Alt rs794728879(C,T;C,T)
Reference rs794728879(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38601637C>G
CLNSRC
CLNACC RCV000183065.2,