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rs794728926

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728926(A;A)
Make rs794728926(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38606687
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728926
ebirs794728926
HLIrs794728926
Exacrs794728926
Varsomers794728926
Maprs794728926
PheGenIrs794728926
hapmaprs794728926
1000 genomesrs794728926
hgdprs794728926
ensemblrs794728926
gopubmedrs794728926
geneviewrs794728926
scholarrs794728926
googlers794728926
pharmgkbrs794728926
gwascentralrs794728926
openSNPrs794728926
23andMers794728926
23andMe allrs794728926
SNP Nexus

SNPshotrs794728926
SNPdbers794728926
MSV3drs794728926
GWAS Ctlgrs794728926
Max Magnitude0
ClinVar
Risk rs794728926(A;A)
Alt rs794728926(A;A)
Reference rs794728926(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38648178C>T
CLNSRC
CLNACC RCV000183171.1,