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rs794728854

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728854(A;A)
Make rs794728854(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38606122
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728854
ebirs794728854
HLIrs794728854
Exacrs794728854
Varsomers794728854
Maprs794728854
PheGenIrs794728854
hapmaprs794728854
1000 genomesrs794728854
hgdprs794728854
ensemblrs794728854
gopubmedrs794728854
geneviewrs794728854
scholarrs794728854
googlers794728854
pharmgkbrs794728854
gwascentralrs794728854
openSNPrs794728854
23andMers794728854
23andMe allrs794728854
SNP Nexus

SNPshotrs794728854
SNPdbers794728854
MSV3drs794728854
GWAS Ctlgrs794728854
Max Magnitude0
ClinVar
Risk rs794728854(A;A)
Alt rs794728854(A;A)
Reference rs794728854(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38647613G>T
CLNSRC
CLNACC RCV000182962.2,