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rs199472876

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472876(A;A)
Make rs199472876(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150958200
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472876
ebirs199472876
HLIrs199472876
Exacrs199472876
Varsomers199472876
Maprs199472876
PheGenIrs199472876
hapmaprs199472876
1000 genomesrs199472876
hgdprs199472876
ensemblrs199472876
gopubmedrs199472876
geneviewrs199472876
scholarrs199472876
googlers199472876
pharmgkbrs199472876
gwascentralrs199472876
openSNPrs199472876
23andMers199472876
23andMe allrs199472876
SNP Nexus

SNPshotrs199472876
SNPdbers199472876
MSV3drs199472876
GWAS Ctlgrs199472876
Max Magnitude0
ClinVar
Risk rs199472876(A;A)
Alt rs199472876(A;A)
Reference rs199472876(G;G)
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.150655288C>T
CLNSRC ClinVar
CLNACC RCV000058256.2, RCV000181767.1,