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rs199472906

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472906(C;T)
Make rs199472906(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150952561
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472906
ebirs199472906
HLIrs199472906
Exacrs199472906
Varsomers199472906
Maprs199472906
PheGenIrs199472906
hapmaprs199472906
1000 genomesrs199472906
hgdprs199472906
ensemblrs199472906
gopubmedrs199472906
geneviewrs199472906
scholarrs199472906
googlers199472906
pharmgkbrs199472906
gwascentralrs199472906
openSNPrs199472906
23andMers199472906
23andMe allrs199472906
SNP Nexus

SNPshotrs199472906
SNPdbers199472906
MSV3drs199472906
GWAS Ctlgrs199472906
Max Magnitude0
ClinVar
Risk rs199472906(T;T)
Alt rs199472906(T;T)
Reference rs199472906(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.150649649G>A
CLNSRC ClinVar
CLNACC RCV000057906.2, RCV000182021.1,