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rs199473018

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473018(A;T)
Make rs199473018(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150947493
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473018
ebirs199473018
HLIrs199473018
Exacrs199473018
Varsomers199473018
Maprs199473018
PheGenIrs199473018
hapmaprs199473018
1000 genomesrs199473018
hgdprs199473018
ensemblrs199473018
gopubmedrs199473018
geneviewrs199473018
scholarrs199473018
googlers199473018
pharmgkbrs199473018
gwascentralrs199473018
openSNPrs199473018
23andMers199473018
23andMe allrs199473018
SNP Nexus

SNPshotrs199473018
SNPdbers199473018
MSV3drs199473018
GWAS Ctlgrs199473018
Max Magnitude0
ClinVar
Risk rs199473018(T;T)
Alt rs199473018(T;T)
Reference rs199473018(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome not provided
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome not provided
Reversed 1
HGVS NC_000007.13:g.150644581T>A
CLNSRC ClinVar
CLNACC RCV000058185.2, RCV000181903.1,