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rs773724817

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs773724817(A;A)
Make rs773724817(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150948861
GeneKCNH2
is asnp
is mentioned by
dbSNPrs773724817
ebirs773724817
HLIrs773724817
Exacrs773724817
Varsomers773724817
Maprs773724817
PheGenIrs773724817
hapmaprs773724817
1000 genomesrs773724817
hgdprs773724817
ensemblrs773724817
gopubmedrs773724817
geneviewrs773724817
scholarrs773724817
googlers773724817
pharmgkbrs773724817
gwascentralrs773724817
openSNPrs773724817
23andMers773724817
23andMe allrs773724817
SNP Nexus

SNPshotrs773724817
SNPdbers773724817
MSV3drs773724817
GWAS Ctlgrs773724817
Max Magnitude0
ClinVar
Risk rs773724817(A;A)
Alt rs773724817(A;A)
Reference rs773724817(G;G)
Significance Pathogenic
Disease Long QT syndrome
Variation info
Gene KCNH2
CLNDBN Long QT syndrome
Reversed 0
HGVS NC_000007.13:g.150645949G>A
CLNSRC
CLNACC RCV000203902.1,