Have questions? Visit https://www.reddit.com/r/SNPedia

rs730880374

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730880374(-;-)
Make rs730880374(-;G)
Make rs730880374(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position150958132
GeneKCNH2
is asnp
is mentioned by
dbSNPrs730880374
ebirs730880374
HLIrs730880374
Exacrs730880374
Varsomers730880374
Maprs730880374
PheGenIrs730880374
hapmaprs730880374
1000 genomesrs730880374
hgdprs730880374
ensemblrs730880374
gopubmedrs730880374
geneviewrs730880374
scholarrs730880374
googlers730880374
pharmgkbrs730880374
gwascentralrs730880374
openSNPrs730880374
23andMers730880374
23andMe allrs730880374
SNP Nexus

SNPshotrs730880374
SNPdbers730880374
MSV3drs730880374
GWAS Ctlgrs730880374
Max Magnitude0
ClinVar
Risk rs730880374(G;G)
Alt rs730880374(G;G)
Reference rs730880374(;)
Significance Probable-Pathogenic
Disease Long QT syndrome 2
Variation info
Gene KCNH2
CLNDBN Long QT syndrome 2
Reversed 1
HGVS NC_000007.13:g.150655221dupC
CLNSRC
CLNACC RCV000157260.1,