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rs767987619

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs767987619(G;T)
Make rs767987619(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32878217
GenePKP2
is asnp
is mentioned by
dbSNPrs767987619
ebirs767987619
HLIrs767987619
Exacrs767987619
Varsomers767987619
Maprs767987619
PheGenIrs767987619
hapmaprs767987619
1000 genomesrs767987619
hgdprs767987619
ensemblrs767987619
gopubmedrs767987619
geneviewrs767987619
scholarrs767987619
googlers767987619
pharmgkbrs767987619
gwascentralrs767987619
openSNPrs767987619
23andMers767987619
23andMe allrs767987619
SNP Nexus

SNPshotrs767987619
SNPdbers767987619
MSV3drs767987619
GWAS Ctlgrs767987619
Max Magnitude0
ClinVar
Risk rs767987619(T;T)
Alt rs767987619(T;T)
Reference rs767987619(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.33031151G>T
CLNSRC
CLNACC RCV000183730.2,