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rs199473073

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473073(C;C)
Make rs199473073(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38613757
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473073
ebirs199473073
HLIrs199473073
Exacrs199473073
Varsomers199473073
Maprs199473073
PheGenIrs199473073
hapmaprs199473073
1000 genomesrs199473073
hgdprs199473073
ensemblrs199473073
gopubmedrs199473073
geneviewrs199473073
scholarrs199473073
googlers199473073
pharmgkbrs199473073
gwascentralrs199473073
openSNPrs199473073
23andMers199473073
23andMe allrs199473073
SNP Nexus

SNPshotrs199473073
SNPdbers199473073
MSV3drs199473073
GWAS Ctlgrs199473073
Max Magnitude0
ClinVar
Risk rs199473073(C;C)
Alt rs199473073(C;C)
Reference rs199473073(T;T)
Significance Pathogenic
Disease Cardiac conduction defect
Variation info
Gene SCN5A
CLNDBN Cardiac conduction defect, nonspecific
Reversed 1
HGVS NC_000003.11:g.38655248A>G
CLNSRC ClinVar
CLNACC RCV000058839.2,