Gene: CRACR2A

Alternate names for this Gene: EFCAB4B

Gene Summary:

Gene is located in Chromosome: 12

Location in Chromosome : 12p13.32

Description of this Gene: calcium release activated channel regulator 2A

Type of Gene: protein-coding

rs10774167 in CRACR2A gene and Leukemia, Myelocytic, Acute PMID 27903959 2017 Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

rs887304 in CRACR2A gene and Liver Cirrhosis PMID 20708005 2010 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.

rs887304 in CRACR2A gene and Non-alcoholic Fatty Liver Disease PMID 20708005 2010 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.

rs242016 in CRACR2A gene and Periodontitis PMID 30284742 2018 Four SNPs on the gene EFCAB4B resulted significantly associated to localized periodontitis (P < 5 × 10<sup>-8</sup> ), with the best hit on the rs242016 SNP (P = 1.5 × 10<sup>-8</sup> ).

rs242016 in CRACR2A gene and Periodontosis PMID 30284742 2018 A genome-wide association study identifies an association between variants in EFCAB4B gene and periodontal disease in an Italian isolated population.