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

rs199472849

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472849(A;A)
Make rs199472849(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150974775
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472849
ebirs199472849
HLIrs199472849
Exacrs199472849
Varsomers199472849
Maprs199472849
PheGenIrs199472849
hapmaprs199472849
1000 genomesrs199472849
hgdprs199472849
ensemblrs199472849
gopubmedrs199472849
geneviewrs199472849
scholarrs199472849
googlers199472849
pharmgkbrs199472849
gwascentralrs199472849
openSNPrs199472849
23andMers199472849
23andMe allrs199472849
SNP Nexus

SNPshotrs199472849
SNPdbers199472849
MSV3drs199472849
GWAS Ctlgrs199472849
Max Magnitude0
ClinVar
Risk rs199472849(A,C;A,C)
Alt rs199472849(A,C;A,C)
Reference rs199472849(G;G)
Significance Probable-Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150671863C>G
CLNSRC ClinVar
CLNACC RCV000058121.2,