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rs1057520597

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520597(A;T)
Make rs1057520597(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position32841029
GenePKP2
is asnp
is mentioned by
dbSNPrs1057520597
dbSNP (old)rs1057520597
ClinGenrs1057520597
ebirs1057520597
HLIrs1057520597
Exacrs1057520597
Gnomadrs1057520597
Varsomers1057520597
Maprs1057520597
PheGenIrs1057520597
Biobankrs1057520597
1000 genomesrs1057520597
hgdprs1057520597
ensemblrs1057520597
gopubmedrs1057520597
geneviewrs1057520597
scholarrs1057520597
googlers1057520597
pharmgkbrs1057520597
gwascentralrs1057520597
openSNPrs1057520597
23andMers1057520597
23andMe allrs1057520597
SNPshotrs1057520597
SNPdbers1057520597
MSV3drs1057520597
GWAS Ctlgrs1057520597
Max Magnitude0
ClinVar
Risk rs1057520597(T;T)
Alt rs1057520597(T;T)
Reference Rs1057520597(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PKP2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.32993963T>A
CLNSRC
CLNACC RCV000438071.1,