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rs794728908

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728908(-;-)
Make rs794728908(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38603891
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728908
ebirs794728908
HLIrs794728908
Exacrs794728908
Varsomers794728908
Maprs794728908
PheGenIrs794728908
hapmaprs794728908
1000 genomesrs794728908
hgdprs794728908
ensemblrs794728908
gopubmedrs794728908
geneviewrs794728908
scholarrs794728908
googlers794728908
pharmgkbrs794728908
gwascentralrs794728908
openSNPrs794728908
23andMers794728908
23andMe allrs794728908
SNP Nexus

SNPshotrs794728908
SNPdbers794728908
MSV3drs794728908
GWAS Ctlgrs794728908
Max Magnitude0
ClinVar
Risk rs794728908(;)
Alt rs794728908(;)
Reference rs794728908(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38645382delT
CLNSRC
CLNACC RCV000183147.1,