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rs786204388

From SNPedia

Orientationminus
Geno Mag Summary
(GAGT;GAGT) 0 common in clinvar
Make rs786204388(-;-)
Make rs786204388(-;GAGT)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32879000
GenePKP2
is asnp
is mentioned by
dbSNPrs786204388
ebirs786204388
HLIrs786204388
Exacrs786204388
Varsomers786204388
Maprs786204388
PheGenIrs786204388
hapmaprs786204388
1000 genomesrs786204388
hgdprs786204388
ensemblrs786204388
gopubmedrs786204388
geneviewrs786204388
scholarrs786204388
googlers786204388
pharmgkbrs786204388
gwascentralrs786204388
openSNPrs786204388
23andMers786204388
23andMe allrs786204388
SNP Nexus

SNPshotrs786204388
SNPdbers786204388
MSV3drs786204388
GWAS Ctlgrs786204388
Max Magnitude0
ClinVar
Risk rs786204388(;)
Alt rs786204388(;)
Reference rs786204388(GAGT;GAGT)
Significance Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene PKP2
CLNDBN Arrhythmogenic right ventricular cardiomyopathy, type 9
Reversed 1
HGVS NC_000012.11:g.33031934_33031937delACTC
CLNSRC
CLNACC RCV000168928.1,