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rs200343561

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs200343561(C;C)
Make rs200343561(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32841047
GenePKP2
is asnp
is mentioned by
dbSNPrs200343561
ebirs200343561
HLIrs200343561
Exacrs200343561
Varsomers200343561
Maprs200343561
PheGenIrs200343561
hapmaprs200343561
1000 genomesrs200343561
hgdprs200343561
ensemblrs200343561
gopubmedrs200343561
geneviewrs200343561
scholarrs200343561
googlers200343561
pharmgkbrs200343561
gwascentralrs200343561
openSNPrs200343561
23andMers200343561
23andMe allrs200343561
SNP Nexus

SNPshotrs200343561
SNPdbers200343561
MSV3drs200343561
GWAS Ctlgrs200343561
Max Magnitude0
ClinVar
Risk rs200343561(C;C)
Alt rs200343561(C;C)
Reference rs200343561(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.32993981T>C
CLNSRC
CLNACC RCV000183749.1,