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rs794728463

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794728463(-;CC)
Make rs794728463(CC;CC)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150947653
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728463
dbSNP (old)rs794728463
ClinGenrs794728463
ebirs794728463
HLIrs794728463
Exacrs794728463
Varsomers794728463
Maprs794728463
PheGenIrs794728463
Biobankrs794728463
1000 genomesrs794728463
hgdprs794728463
ensemblrs794728463
gopubmedrs794728463
geneviewrs794728463
scholarrs794728463
googlers794728463
pharmgkbrs794728463
gwascentralrs794728463
openSNPrs794728463
23andMers794728463
23andMe allrs794728463
SNP Nexus

SNPshotrs794728463
SNPdbers794728463
MSV3drs794728463
GWAS Ctlgrs794728463
Max Magnitude0
ClinVar
Risk rs794728463(CC;CC)
Alt rs794728463(CC;CC)
Reference Rs794728463(-;-)
Significance Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Cardiac arrhythmia
Reversed 1
HGVS NC_000007.13:g.150644742_150644743dupGG
CLNSRC
CLNACC RCV000182002.1,