Have questions? Visit https://www.reddit.com/r/SNPedia

rs199472921

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472921(C;C)
Make rs199472921(C;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951712
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472921
ebirs199472921
HLIrs199472921
Exacrs199472921
Varsomers199472921
Maprs199472921
PheGenIrs199472921
hapmaprs199472921
1000 genomesrs199472921
hgdprs199472921
ensemblrs199472921
gopubmedrs199472921
geneviewrs199472921
scholarrs199472921
googlers199472921
pharmgkbrs199472921
gwascentralrs199472921
openSNPrs199472921
23andMers199472921
23andMe allrs199472921
SNP Nexus

SNPshotrs199472921
SNPdbers199472921
MSV3drs199472921
GWAS Ctlgrs199472921
Max Magnitude0
ClinVar
Risk rs199472921(A,C;A,C)
Alt rs199472921(A,C;A,C)
Reference rs199472921(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.150648800C>G; NC_000007.13:g.150648800C>T
CLNSRC ClinVar
CLNACC RCV000057940.2, RCV000057939.2, RCV000181805.2,