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rs794728850

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728850(A;C)
Make rs794728850(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38613744
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728850
ebirs794728850
HLIrs794728850
Exacrs794728850
Varsomers794728850
Maprs794728850
PheGenIrs794728850
hapmaprs794728850
1000 genomesrs794728850
hgdprs794728850
ensemblrs794728850
gopubmedrs794728850
geneviewrs794728850
scholarrs794728850
googlers794728850
pharmgkbrs794728850
gwascentralrs794728850
openSNPrs794728850
23andMers794728850
23andMe allrs794728850
SNP Nexus

SNPshotrs794728850
SNPdbers794728850
MSV3drs794728850
GWAS Ctlgrs794728850
Max Magnitude0
ClinVar
Risk rs794728850(C;C)
Alt rs794728850(C;C)
Reference rs794728850(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38655235T>G
CLNSRC
CLNACC RCV000182944.1,