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rs199472829

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199472829(A;G)
Make rs199472829(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150974936
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472829
ebirs199472829
HLIrs199472829
Exacrs199472829
Varsomers199472829
Maprs199472829
PheGenIrs199472829
hapmaprs199472829
1000 genomesrs199472829
hgdprs199472829
ensemblrs199472829
gopubmedrs199472829
geneviewrs199472829
scholarrs199472829
googlers199472829
pharmgkbrs199472829
gwascentralrs199472829
openSNPrs199472829
23andMers199472829
23andMe allrs199472829
SNP Nexus

SNPshotrs199472829
SNPdbers199472829
MSV3drs199472829
GWAS Ctlgrs199472829
Max Magnitude0
ClinVar
Risk rs199472829(G;G)
Alt rs199472829(G;G)
Reference rs199472829(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150672024T>C
CLNSRC ClinVar
CLNACC RCV000058261.2,