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

rs587777907

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777907(A;T)
Make rs587777907(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position150958319
GeneKCNH2
is asnp
is mentioned by
dbSNPrs587777907
ebirs587777907
HLIrs587777907
Exacrs587777907
Varsomers587777907
Maprs587777907
PheGenIrs587777907
hapmaprs587777907
1000 genomesrs587777907
hgdprs587777907
ensemblrs587777907
gopubmedrs587777907
geneviewrs587777907
scholarrs587777907
googlers587777907
pharmgkbrs587777907
gwascentralrs587777907
openSNPrs587777907
23andMers587777907
23andMe allrs587777907
SNP Nexus

SNPshotrs587777907
SNPdbers587777907
MSV3drs587777907
GWAS Ctlgrs587777907
Max Magnitude0
ClinVar
Risk rs587777907(T;T)
Alt rs587777907(T;T)
Reference rs587777907(A;A)
Significance Pathogenic
Disease Long QT syndrome 2
Variation info
Gene KCNH2
CLNDBN Long QT syndrome 2
Reversed 1
HGVS NC_000007.13:g.150655407T>A
CLNSRC
CLNACC RCV000144957.2,