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rs786204101

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786204101(-;-)
Make rs786204101(-;C)
Make rs786204101(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150947670
GeneKCNH2
is asnp
is mentioned by
dbSNPrs786204101
ebirs786204101
HLIrs786204101
Exacrs786204101
Varsomers786204101
Maprs786204101
PheGenIrs786204101
hapmaprs786204101
1000 genomesrs786204101
hgdprs786204101
ensemblrs786204101
gopubmedrs786204101
geneviewrs786204101
scholarrs786204101
googlers786204101
pharmgkbrs786204101
gwascentralrs786204101
openSNPrs786204101
23andMers786204101
23andMe allrs786204101
SNP Nexus

SNPshotrs786204101
SNPdbers786204101
MSV3drs786204101
GWAS Ctlgrs786204101
Max Magnitude0
ClinVar
Risk rs786204101(C;C)
Alt rs786204101(C;C)
Reference rs786204101(;)
Significance Pathogenic
Disease Long QT syndrome Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Long QT syndrome Cardiac arrhythmia
Reversed 1
HGVS NC_000007.13:g.150644759dupG
CLNSRC
CLNACC RCV000168023.1, RCV000182001.1,