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rs373222905

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs373222905(C;T)
Make rs373222905(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32878332
GenePKP2
is asnp
is mentioned by
dbSNPrs373222905
ebirs373222905
HLIrs373222905
Exacrs373222905
Varsomers373222905
Maprs373222905
PheGenIrs373222905
hapmaprs373222905
1000 genomesrs373222905
hgdprs373222905
ensemblrs373222905
gopubmedrs373222905
geneviewrs373222905
scholarrs373222905
googlers373222905
pharmgkbrs373222905
gwascentralrs373222905
openSNPrs373222905
23andMers373222905
23andMe allrs373222905
SNP Nexus

SNPshotrs373222905
SNPdbers373222905
MSV3drs373222905
GWAS Ctlgrs373222905
Max Magnitude0
ClinVar
Risk rs373222905(T;T)
Alt rs373222905(T;T)
Reference rs373222905(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.33031266C>T
CLNSRC
CLNACC RCV000183728.1,