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rs794728470

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794728470(-;GGGCGACG)
Make rs794728470(GGGCGACG;GGGCGACG)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150947367
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728470
ClinGenrs794728470
ebirs794728470
HLIrs794728470
Exacrs794728470
Varsomers794728470
Maprs794728470
PheGenIrs794728470
hapmaprs794728470
1000 genomesrs794728470
hgdprs794728470
ensemblrs794728470
gopubmedrs794728470
geneviewrs794728470
scholarrs794728470
googlers794728470
pharmgkbrs794728470
gwascentralrs794728470
openSNPrs794728470
23andMers794728470
23andMe allrs794728470
SNP Nexus

SNPshotrs794728470
SNPdbers794728470
MSV3drs794728470
GWAS Ctlgrs794728470
Max Magnitude0
ClinVar
Risk rs794728470(GGGCGACG;GGGCGACG)
Alt rs794728470(GGGCGACG;GGGCGACG)
Reference Rs794728470(;)
Significance Pathogenic
Disease Cardiac arrhythmia Long QT syndrome
Variation info
Gene KCNH2
CLNDBN Cardiac arrhythmia Long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150644456_150644463dupCGTCGCCC
CLNSRC
CLNACC RCV000182010.1, RCV000231614.1,