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rs138498207

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs138498207(A;A)
Make rs138498207(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150950195
GeneKCNH2
is asnp
is mentioned by
dbSNPrs138498207
ebirs138498207
HLIrs138498207
Exacrs138498207
Varsomers138498207
Maprs138498207
PheGenIrs138498207
hapmaprs138498207
1000 genomesrs138498207
hgdprs138498207
ensemblrs138498207
gopubmedrs138498207
geneviewrs138498207
scholarrs138498207
googlers138498207
pharmgkbrs138498207
gwascentralrs138498207
openSNPrs138498207
23andMers138498207
23andMe allrs138498207
SNP Nexus

SNPshotrs138498207
SNPdbers138498207
MSV3drs138498207
GWAS Ctlgrs138498207
Max Magnitude0
ClinVar
Risk rs138498207(A;A)
Alt rs138498207(A;A)
Reference rs138498207(G;G)
Significance Other
Disease Congenital long QT syndrome Long QT syndrome Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome Long QT syndrome Cardiac arrhythmia
Reversed 0
HGVS NC_000007.13:g.150647283G>A
CLNSRC ClinVar University of Washington
CLNACC RCV000058113.2, RCV000148535.2, RCV000181852.1,