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rs786205476

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205476(C;C)
Make rs786205476(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32822587
GenePKP2
is asnp
is mentioned by
dbSNPrs786205476
ebirs786205476
HLIrs786205476
Exacrs786205476
Varsomers786205476
Maprs786205476
PheGenIrs786205476
hapmaprs786205476
1000 genomesrs786205476
hgdprs786205476
ensemblrs786205476
gopubmedrs786205476
geneviewrs786205476
scholarrs786205476
googlers786205476
pharmgkbrs786205476
gwascentralrs786205476
openSNPrs786205476
23andMers786205476
23andMe allrs786205476
SNP Nexus

SNPshotrs786205476
SNPdbers786205476
MSV3drs786205476
GWAS Ctlgrs786205476
Max Magnitude0
ClinVar
Risk rs786205476(C;C)
Alt rs786205476(C;C)
Reference rs786205476(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.32975521C>G
CLNSRC
CLNACC RCV000171211.1,