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rs794728464

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794728464(-;AGGC)
Make rs794728464(AGGC;AGGC)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150947512
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728464
ClinGenrs794728464
ebirs794728464
HLIrs794728464
Exacrs794728464
Varsomers794728464
Maprs794728464
PheGenIrs794728464
hapmaprs794728464
1000 genomesrs794728464
hgdprs794728464
ensemblrs794728464
gopubmedrs794728464
geneviewrs794728464
scholarrs794728464
googlers794728464
pharmgkbrs794728464
gwascentralrs794728464
openSNPrs794728464
23andMers794728464
23andMe allrs794728464
SNP Nexus

SNPshotrs794728464
SNPdbers794728464
MSV3drs794728464
GWAS Ctlgrs794728464
Max Magnitude0
ClinVar
Risk rs794728464(AGGC;AGGC)
Alt rs794728464(AGGC;AGGC)
Reference Rs794728464(-;-)
Significance Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Cardiac arrhythmia
Reversed 1
HGVS NC_000007.13:g.150644601_150644604dupGCCT
CLNSRC
CLNACC RCV000182003.1,