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rs143512106

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs143512106(A;A)
Make rs143512106(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150948483
GeneKCNH2
is asnp
is mentioned by
dbSNPrs143512106
ebirs143512106
HLIrs143512106
Exacrs143512106
Varsomers143512106
Maprs143512106
PheGenIrs143512106
hapmaprs143512106
1000 genomesrs143512106
hgdprs143512106
ensemblrs143512106
gopubmedrs143512106
geneviewrs143512106
scholarrs143512106
googlers143512106
pharmgkbrs143512106
gwascentralrs143512106
openSNPrs143512106
23andMers143512106
23andMe allrs143512106
SNP Nexus

SNPshotrs143512106
SNPdbers143512106
MSV3drs143512106
GWAS Ctlgrs143512106
Max Magnitude0
ClinVar
Risk rs143512106(A,T;A,T)
Alt rs143512106(A,T;A,T)
Reference rs143512106(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome Long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome Long QT syndrome
Reversed 0
HGVS NC_000007.13:g.150645571G>A
CLNSRC ClinVar University of Washington
CLNACC RCV000058147.2, RCV000148524.1,