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rs199473669

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473669(A;A)
Make rs199473669(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150947864
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473669
ebirs199473669
HLIrs199473669
Exacrs199473669
Varsomers199473669
Maprs199473669
PheGenIrs199473669
hapmaprs199473669
1000 genomesrs199473669
hgdprs199473669
ensemblrs199473669
gopubmedrs199473669
geneviewrs199473669
scholarrs199473669
googlers199473669
pharmgkbrs199473669
gwascentralrs199473669
openSNPrs199473669
23andMers199473669
23andMe allrs199473669
SNP Nexus

SNPshotrs199473669
SNPdbers199473669
MSV3drs199473669
GWAS Ctlgrs199473669
Max Magnitude0
ClinVar
Risk rs199473669(A;A)
Alt rs199473669(A;A)
Reference rs199473669(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.150644952C>T
CLNSRC ClinVar
CLNACC RCV000058153.2, RCV000181883.2,