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rs794728500

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;C) 5 Romano-Ward Long QT Syndrome
(C;C) 0 common in clinvar
(I;I) 0 common genotype


Make rs794728500(-;-)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150951013
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728500
dbSNP (classic)rs794728500
ClinGenrs794728500
ebirs794728500
HLIrs794728500
Exacrs794728500
Gnomadrs794728500
Varsomers794728500
LitVarrs794728500
Maprs794728500
PheGenIrs794728500
Biobankrs794728500
1000 genomesrs794728500
hgdprs794728500
ensemblrs794728500
geneviewrs794728500
scholarrs794728500
googlers794728500
pharmgkbrs794728500
gwascentralrs794728500
openSNPrs794728500
23andMers794728500
SNPshotrs794728500
SNPdbers794728500
MSV3drs794728500
GWAS Ctlgrs794728500
Max Magnitude5
ClinVar
Risk rs794728500(-;-)
Alt rs794728500(-;-)
Reference Rs794728500(C;C)
Significance Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Cardiac arrhythmia
Reversed 1
HGVS NC_000007.13:g.150648101delG
CLNSRC
CLNACC RCV000182059.1,