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rs794728887

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728887(A;G)
Make rs794728887(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38555736
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728887
ebirs794728887
HLIrs794728887
Exacrs794728887
Varsomers794728887
Maprs794728887
PheGenIrs794728887
hapmaprs794728887
1000 genomesrs794728887
hgdprs794728887
ensemblrs794728887
gopubmedrs794728887
geneviewrs794728887
scholarrs794728887
googlers794728887
pharmgkbrs794728887
gwascentralrs794728887
openSNPrs794728887
23andMers794728887
23andMe allrs794728887
SNP Nexus

SNPshotrs794728887
SNPdbers794728887
MSV3drs794728887
GWAS Ctlgrs794728887
Max Magnitude0
ClinVar
Risk rs794728887(G;G)
Alt rs794728887(G;G)
Reference rs794728887(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38597227T>C
CLNSRC
CLNACC RCV000183078.1,