rs10891290
×
Entrez Id:
5519
Gene Symbol:
PPP2R1B
PPP2R1B
Waist-Hip Ratio
T
0.700
GeneticVariation
GWASCAT
Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry.
30239722
2019
rs4936675
×
Entrez Id:
5519
Gene Symbol:
PPP2R1B
PPP2R1B
Finding of Mean Corpuscular Hemoglobin
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs11213999
×
Entrez Id:
5519
Gene Symbol:
PPP2R1B
PPP2R1B
Wrinkled face
A
0.700
GeneticVariation
GWASCAT
Facial Wrinkles in Europeans: A Genome-Wide Association Study.
29555444
2018
rs12362593
PPP2R1B;SIK2
Diastolic blood pressure
C
0.700
GeneticVariation
GWASCAT
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
30224653
2018
rs17565975
PPP2R1B;SIK2
mathematical ability
A
0.700
GeneticVariation
GWASCAT
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
30038396
2018
rs643506
×
Entrez Id:
5519
Gene Symbol:
PPP2R1B
PPP2R1B
Breast Carcinoma
G
0.700
GeneticVariation
GWASCAT
Association analysis identifies 65 new breast cancer risk loci.
29059683
2017
rs7937682
PPP2R1B;SIK2
Cholangitis, Sclerosing
C
0.700
GeneticVariation
GWASCAT
Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease.
27992413
2017
rs7937682
PPP2R1B;SIK2
Cholangitis, Sclerosing
G
0.700
GeneticVariation
GWASCAT
Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis.
23603763
2013
rs7937682
PPP2R1B;SIK2
Primary sclerosing cholangitis
0.700
GeneticVariation
GWASDB
Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis.
23603763
2013
rs1318084062
×
Entrez Id:
5519
Gene Symbol:
PPP2R1B
PPP2R1B
Adenocarcinoma of colon
0.700
GeneticVariation
UNIPROT
rs142771326
×
Entrez Id:
5519
Gene Symbol:
PPP2R1B
PPP2R1B
Malignant neoplasm of lung
0.700
GeneticVariation
UNIPROT
rs1442893893
×
Entrez Id:
5519
Gene Symbol:
PPP2R1B
PPP2R1B
Colorectal Carcinoma
0.700
GeneticVariation
UNIPROT
rs1805076
×
Entrez Id:
5519
Gene Symbol:
PPP2R1B
PPP2R1B
Malignant neoplasm of lung
0.700
GeneticVariation
UNIPROT
rs1805076
×
Entrez Id:
5519
Gene Symbol:
PPP2R1B
PPP2R1B
Carcinoma of lung
T
0.700
CausalMutation
CLINVAR
rs973682124
×
Entrez Id:
5519
Gene Symbol:
PPP2R1B
PPP2R1B
Malignant neoplasm of lung
0.700
GeneticVariation
UNIPROT
rs1805076
×
Entrez Id:
5519
Gene Symbol:
PPP2R1B
PPP2R1B
Breast Carcinoma
0.010
GeneticVariation
BEFREE
The frequency of the G90D polymorphism in br</span>east cancer patients was significantly higher in cases (3%) than in controls (0.3%).
16276521
2006
rs1805076
×
Entrez Id:
5519
Gene Symbol:
PPP2R1B
PPP2R1B
Primary malignant neoplasm
0.010
GeneticVariation
BEFREE
One of these mutations results in an alteration of glycine 90 to aspartic acid (G90D ), which has been found in both tumor and genomic DNA, raising the possibility that it is associated with an increased risk for cancer .
16276521
2006
rs1805076
×
Entrez Id:
5519
Gene Symbol:
PPP2R1B
PPP2R1B
Malignant neoplasm of breast
0.010
GeneticVariation
BEFREE
The frequency of the G90D polymorphism in breast cancer patients was significantly higher in cases (3%) than in controls (0.3%).
16276521
2006
rs1805076
×
Entrez Id:
5519
Gene Symbol:
PPP2R1B
PPP2R1B
Malignant Neoplasms
0.010
GeneticVariation
BEFREE
One of these mutations results in an alteration of glycine 90 to aspartic acid (G90D ), which has been found in both tumor and genomic DNA, raising the possibility that it is associated with an increased risk for cancer .
16276521
2006
rs1805076
×
Entrez Id:
5519
Gene Symbol:
PPP2R1B
PPP2R1B
Neoplasms
0.010
GeneticVariation
BEFREE
One of these mutations results in an alteration of glycine 90 to aspartic acid (G90D ), which has been found in both tumor and genomic DNA, raising the possibility that it is associated with an increased risk for cancer.
16276521
2006