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rs199473515

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473515(A;A)
Make rs199473515(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951801
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473515
ebirs199473515
HLIrs199473515
Exacrs199473515
Varsomers199473515
Maprs199473515
PheGenIrs199473515
hapmaprs199473515
1000 genomesrs199473515
hgdprs199473515
ensemblrs199473515
gopubmedrs199473515
geneviewrs199473515
scholarrs199473515
googlers199473515
pharmgkbrs199473515
gwascentralrs199473515
openSNPrs199473515
23andMers199473515
23andMe allrs199473515
SNP Nexus

SNPshotrs199473515
SNPdbers199473515
MSV3drs199473515
GWAS Ctlgrs199473515
Max Magnitude0
ClinVar
Risk rs199473515(A;A)
Alt rs199473515(A;A)
Reference rs199473515(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.150648889C>T
CLNSRC ClinVar
CLNACC RCV000057928.2,