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rs864622309

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864622309(-;-)
Make rs864622309(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150947386
GeneKCNH2
is asnp
is mentioned by
dbSNPrs864622309
dbSNP (old)rs864622309
ClinGenrs864622309
ebirs864622309
HLIrs864622309
Exacrs864622309
Gnomadrs864622309
Varsomers864622309
Maprs864622309
PheGenIrs864622309
Biobankrs864622309
1000 genomesrs864622309
hgdprs864622309
ensemblrs864622309
gopubmedrs864622309
geneviewrs864622309
scholarrs864622309
googlers864622309
pharmgkbrs864622309
gwascentralrs864622309
openSNPrs864622309
23andMers864622309
23andMe allrs864622309
SNP Nexus

SNPshotrs864622309
SNPdbers864622309
MSV3drs864622309
GWAS Ctlgrs864622309
Max Magnitude0
ClinVar
Risk rs864622309(-;-)
Alt rs864622309(-;-)
Reference Rs864622309(C;C)
Significance Pathogenic
Disease Long QT syndrome not provided
Variation info
Gene KCNH2
CLNDBN Long QT syndrome not provided
Reversed 1
HGVS NC_000007.13:g.150644474delG
CLNSRC
CLNACC RCV000204772.2, RCV000413486.1,