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rs199472900

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472900(A;A)
Make rs199472900(A;C)
ReferenceGRCh38 38.1/142
Chromosome7
Position150952689
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472900
ebirs199472900
HLIrs199472900
Exacrs199472900
Varsomers199472900
Maprs199472900
PheGenIrs199472900
hapmaprs199472900
1000 genomesrs199472900
hgdprs199472900
ensemblrs199472900
gopubmedrs199472900
geneviewrs199472900
scholarrs199472900
googlers199472900
pharmgkbrs199472900
gwascentralrs199472900
openSNPrs199472900
23andMers199472900
23andMe allrs199472900
SNP Nexus

SNPshotrs199472900
SNPdbers199472900
MSV3drs199472900
GWAS Ctlgrs199472900
Max Magnitude0
ClinVar
Risk rs199472900(A;A)
Alt rs199472900(A;A)
Reference rs199472900(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150649777G>T
CLNSRC ClinVar
CLNACC RCV000057890.2,