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.