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rs766209297

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs766209297(A;A)
Make rs766209297(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32868935
GenePKP2
is asnp
is mentioned by
dbSNPrs766209297
ebirs766209297
HLIrs766209297
Exacrs766209297
Varsomers766209297
Maprs766209297
PheGenIrs766209297
hapmaprs766209297
1000 genomesrs766209297
hgdprs766209297
ensemblrs766209297
gopubmedrs766209297
geneviewrs766209297
scholarrs766209297
googlers766209297
pharmgkbrs766209297
gwascentralrs766209297
openSNPrs766209297
23andMers766209297
23andMe allrs766209297
SNP Nexus

SNPshotrs766209297
SNPdbers766209297
MSV3drs766209297
GWAS Ctlgrs766209297
Max Magnitude0
ClinVar
Risk rs766209297(A;A)
Alt rs766209297(A;A)
Reference rs766209297(G;G)
Significance Pathogenic
Disease not provided Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene PKP2
CLNDBN not provided Arrhythmogenic right ventricular cardiomyopathy
Reversed 0
HGVS NC_000012.11:g.33021869G>A
CLNSRC
CLNACC RCV000183736.1, RCV000208105.1,