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rs199472888

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472888(C;T)
Make rs199472888(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150957418
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472888
ebirs199472888
HLIrs199472888
Exacrs199472888
Varsomers199472888
Maprs199472888
PheGenIrs199472888
hapmaprs199472888
1000 genomesrs199472888
hgdprs199472888
ensemblrs199472888
gopubmedrs199472888
geneviewrs199472888
scholarrs199472888
googlers199472888
pharmgkbrs199472888
gwascentralrs199472888
openSNPrs199472888
23andMers199472888
23andMe allrs199472888
SNP Nexus

SNPshotrs199472888
SNPdbers199472888
MSV3drs199472888
GWAS Ctlgrs199472888
Max Magnitude0
ClinVar
Risk rs199472888(T;T)
Alt rs199472888(T;T)
Reference rs199472888(C;C)
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.150654506G>A
CLNSRC ClinVar
CLNACC RCV000057868.2, RCV000181776.1,