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rs794728465

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794728465(-;C)
Make rs794728465(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150947400
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728465
dbSNP (old)rs794728465
ClinGenrs794728465
ebirs794728465
HLIrs794728465
Exacrs794728465
Gnomadrs794728465
Varsomers794728465
Maprs794728465
PheGenIrs794728465
Biobankrs794728465
1000 genomesrs794728465
hgdprs794728465
ensemblrs794728465
gopubmedrs794728465
geneviewrs794728465
scholarrs794728465
googlers794728465
pharmgkbrs794728465
gwascentralrs794728465
openSNPrs794728465
23andMers794728465
23andMe allrs794728465
SNP Nexus

SNPshotrs794728465
SNPdbers794728465
MSV3drs794728465
GWAS Ctlgrs794728465
Max Magnitude0
ClinVar
Risk rs794728465(C;C)
Alt rs794728465(C;C)
Reference Rs794728465(-;-)
Significance Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Cardiac arrhythmia
Reversed 1
HGVS NC_000007.13:g.150644489dupG
CLNSRC
CLNACC RCV000182005.1,