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rs199473121

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473121(A;A)
Make rs199473121(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position38603998
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473121
ebirs199473121
HLIrs199473121
Exacrs199473121
Varsomers199473121
Maprs199473121
PheGenIrs199473121
hapmaprs199473121
1000 genomesrs199473121
hgdprs199473121
ensemblrs199473121
gopubmedrs199473121
geneviewrs199473121
scholarrs199473121
googlers199473121
pharmgkbrs199473121
gwascentralrs199473121
openSNPrs199473121
23andMers199473121
23andMe allrs199473121
SNP Nexus

SNPshotrs199473121
SNPdbers199473121
MSV3drs199473121
GWAS Ctlgrs199473121
Max Magnitude0
ClinVar
Risk rs199473121(A;A)
Alt rs199473121(A;A)
Reference rs199473121(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38645489C>T
CLNSRC ClinVar
CLNACC RCV000058435.2,