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rs794728846

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728846(A;A)
Make rs794728846(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38620972
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728846
ebirs794728846
HLIrs794728846
Exacrs794728846
Varsomers794728846
Maprs794728846
PheGenIrs794728846
hapmaprs794728846
1000 genomesrs794728846
hgdprs794728846
ensemblrs794728846
gopubmedrs794728846
geneviewrs794728846
scholarrs794728846
googlers794728846
pharmgkbrs794728846
gwascentralrs794728846
openSNPrs794728846
23andMers794728846
23andMe allrs794728846
SNP Nexus

SNPshotrs794728846
SNPdbers794728846
MSV3drs794728846
GWAS Ctlgrs794728846
Max Magnitude0
ClinVar
Risk rs794728846(A;A)
Alt rs794728846(A;A)
Reference rs794728846(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38662463C>T
CLNSRC
CLNACC RCV000182928.1,