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rs143397927

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs143397927(A;G)
Make rs143397927(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome12
Position32850852
GenePKP2
is asnp
is mentioned by
dbSNPrs143397927
dbSNP (old)rs143397927
ClinGenrs143397927
ebirs143397927
HLIrs143397927
Exacrs143397927
Gnomadrs143397927
Varsomers143397927
Maprs143397927
PheGenIrs143397927
Biobankrs143397927
1000 genomesrs143397927
hgdprs143397927
ensemblrs143397927
gopubmedrs143397927
geneviewrs143397927
scholarrs143397927
googlers143397927
pharmgkbrs143397927
gwascentralrs143397927
openSNPrs143397927
23andMers143397927
23andMe allrs143397927
SNPshotrs143397927
SNPdbers143397927
MSV3drs143397927
GWAS Ctlgrs143397927
Max Magnitude0
ClinVar
Risk rs143397927(G;G) rs143397927(T;T)
Alt rs143397927(G;G) rs143397927(T;T)
Reference Rs143397927(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.33003786A>T
CLNSRC
CLNACC RCV000254703.2,