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rs199473491

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473491(A;A)
Make rs199473491(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150974860
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473491
ebirs199473491
HLIrs199473491
Exacrs199473491
Varsomers199473491
Maprs199473491
PheGenIrs199473491
hapmaprs199473491
1000 genomesrs199473491
hgdprs199473491
ensemblrs199473491
gopubmedrs199473491
geneviewrs199473491
scholarrs199473491
googlers199473491
pharmgkbrs199473491
gwascentralrs199473491
openSNPrs199473491
23andMers199473491
23andMe allrs199473491
SNP Nexus

SNPshotrs199473491
SNPdbers199473491
MSV3drs199473491
GWAS Ctlgrs199473491
Max Magnitude0
ClinVar
Risk rs199473491(A;A)
Alt rs199473491(A;A)
Reference rs199473491(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150671948C>T
CLNSRC ClinVar
CLNACC RCV000057926.2,