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

rs199473415

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473415(A;A)
Make rs199473415(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150974827
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473415
ebirs199473415
HLIrs199473415
Exacrs199473415
Varsomers199473415
Maprs199473415
PheGenIrs199473415
hapmaprs199473415
1000 genomesrs199473415
hgdprs199473415
ensemblrs199473415
gopubmedrs199473415
geneviewrs199473415
scholarrs199473415
googlers199473415
pharmgkbrs199473415
gwascentralrs199473415
openSNPrs199473415
23andMers199473415
23andMe allrs199473415
SNP Nexus

SNPshotrs199473415
SNPdbers199473415
MSV3drs199473415
GWAS Ctlgrs199473415
Max Magnitude0
ClinVar
Risk rs199473415(A;A)
Alt rs199473415(A;A)
Reference rs199473415(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150671915C>T
CLNSRC ClinVar
CLNACC RCV000058054.2,