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rs794728943

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728943(-;-)
Make rs794728943(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38557286
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728943
ebirs794728943
HLIrs794728943
Exacrs794728943
Varsomers794728943
Maprs794728943
PheGenIrs794728943
hapmaprs794728943
1000 genomesrs794728943
hgdprs794728943
ensemblrs794728943
gopubmedrs794728943
geneviewrs794728943
scholarrs794728943
googlers794728943
pharmgkbrs794728943
gwascentralrs794728943
openSNPrs794728943
23andMers794728943
23andMe allrs794728943
SNP Nexus

SNPshotrs794728943
SNPdbers794728943
MSV3drs794728943
GWAS Ctlgrs794728943
Max Magnitude0
ClinVar
Risk rs794728943(;)
Alt rs794728943(;)
Reference rs794728943(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38598777delT
CLNSRC
CLNACC RCV000183205.1,