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rs794728903

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728903(A;T)
Make rs794728903(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38550437
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728903
ebirs794728903
HLIrs794728903
Exacrs794728903
Varsomers794728903
Maprs794728903
PheGenIrs794728903
hapmaprs794728903
1000 genomesrs794728903
hgdprs794728903
ensemblrs794728903
gopubmedrs794728903
geneviewrs794728903
scholarrs794728903
googlers794728903
pharmgkbrs794728903
gwascentralrs794728903
openSNPrs794728903
23andMers794728903
23andMe allrs794728903
SNP Nexus

SNPshotrs794728903
SNPdbers794728903
MSV3drs794728903
GWAS Ctlgrs794728903
Max Magnitude0
ClinVar
Risk rs794728903(T;T)
Alt rs794728903(T;T)
Reference rs794728903(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38591928T>A
CLNSRC
CLNACC RCV000183139.1,