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rs199472968

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472968(A;A)
Make rs199472968(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951484
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472968
ClinGenrs199472968
ebirs199472968
HLIrs199472968
Exacrs199472968
Varsomers199472968
Maprs199472968
PheGenIrs199472968
hapmaprs199472968
1000 genomesrs199472968
hgdprs199472968
ensemblrs199472968
gopubmedrs199472968
geneviewrs199472968
scholarrs199472968
googlers199472968
pharmgkbrs199472968
gwascentralrs199472968
openSNPrs199472968
23andMers199472968
23andMe allrs199472968
SNP Nexus

SNPshotrs199472968
SNPdbers199472968
MSV3drs199472968
GWAS Ctlgrs199472968
Max Magnitude0
ClinVar
Risk rs199472968(A;A)
Alt rs199472968(A;A)
Reference Rs199472968(G;G)
Significance Untested
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150648572C>T
CLNSRC UniProtKB (protein)
CLNACC RCV000058048.3,