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

rs199473668

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473668(A;A)
Make rs199473668(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150948455
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473668
ebirs199473668
HLIrs199473668
Exacrs199473668
Varsomers199473668
Maprs199473668
PheGenIrs199473668
hapmaprs199473668
1000 genomesrs199473668
hgdprs199473668
ensemblrs199473668
gopubmedrs199473668
geneviewrs199473668
scholarrs199473668
googlers199473668
pharmgkbrs199473668
gwascentralrs199473668
openSNPrs199473668
23andMers199473668
23andMe allrs199473668
SNP Nexus

SNPshotrs199473668
SNPdbers199473668
MSV3drs199473668
GWAS Ctlgrs199473668
Max Magnitude0
ClinVar
Risk rs199473668(A,T;A,T)
Alt rs199473668(A,T;A,T)
Reference rs199473668(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome Cardiac arrhythmia
Reversed 1
HGVS NC_000007.13:g.150645543C>A
CLNSRC ClinVar
CLNACC RCV000058150.2, RCV000181881.1,