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rs794728849

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728849(C;T)
Make rs794728849(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38613782
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728849
ebirs794728849
HLIrs794728849
Exacrs794728849
Varsomers794728849
Maprs794728849
PheGenIrs794728849
hapmaprs794728849
1000 genomesrs794728849
hgdprs794728849
ensemblrs794728849
gopubmedrs794728849
geneviewrs794728849
scholarrs794728849
googlers794728849
pharmgkbrs794728849
gwascentralrs794728849
openSNPrs794728849
23andMers794728849
23andMe allrs794728849
SNP Nexus

SNPshotrs794728849
SNPdbers794728849
MSV3drs794728849
GWAS Ctlgrs794728849
Max Magnitude0
ClinVar
Risk rs794728849(G,T;G,T)
Alt rs794728849(G,T;G,T)
Reference rs794728849(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38655273G>A; NC_000003.11:g.38655273G>C
CLNSRC
CLNACC RCV000182937.1, RCV000182940.1,