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rs794728934

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728934(C;C)
Make rs794728934(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38557225
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728934
ebirs794728934
HLIrs794728934
Exacrs794728934
Varsomers794728934
Maprs794728934
PheGenIrs794728934
hapmaprs794728934
1000 genomesrs794728934
hgdprs794728934
ensemblrs794728934
gopubmedrs794728934
geneviewrs794728934
scholarrs794728934
googlers794728934
pharmgkbrs794728934
gwascentralrs794728934
openSNPrs794728934
23andMers794728934
23andMe allrs794728934
SNP Nexus

SNPshotrs794728934
SNPdbers794728934
MSV3drs794728934
GWAS Ctlgrs794728934
Max Magnitude0
ClinVar
Risk rs794728934(A,C;A,C)
Alt rs794728934(A,C;A,C)
Reference rs794728934(T;T)
Significance Pathogenic
Disease not provided not specified
Variation info
Gene SCN5A
CLNDBN not provided not specified
Reversed 1
HGVS NC_000003.11:g.38598716A>G; NC_000003.11:g.38598716A>T
CLNSRC
CLNACC RCV000183187.1, RCV000215366.1,