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rs199473184

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473184(C;T)
Make rs199473184(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38581137
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473184
ebirs199473184
HLIrs199473184
Exacrs199473184
Varsomers199473184
Maprs199473184
PheGenIrs199473184
hapmaprs199473184
1000 genomesrs199473184
hgdprs199473184
ensemblrs199473184
gopubmedrs199473184
geneviewrs199473184
scholarrs199473184
googlers199473184
pharmgkbrs199473184
gwascentralrs199473184
openSNPrs199473184
23andMers199473184
23andMe allrs199473184
SNP Nexus

SNPshotrs199473184
SNPdbers199473184
MSV3drs199473184
GWAS Ctlgrs199473184
Max Magnitude0
ClinVar
Risk rs199473184(T;T)
Alt rs199473184(T;T)
Reference rs199473184(C;C)
Significance Pathogenic
Disease Cardiac conduction defect
Variation info
Gene SCN5A
CLNDBN Cardiac conduction defect, nonspecific
Reversed 1
HGVS NC_000003.11:g.38622628G>A
CLNSRC ClinVar
CLNACC RCV000058544.2,