ARID3B, AT-rich interaction domain 3B, 10620

N. diseases: 46; N. variants: 5
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs8025068
rs8025068
Entrez Id: 10620
Gene Symbol: ARID3B
ARID3B
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs11072494
rs11072494
Entrez Id: 10620
Gene Symbol: ARID3B
ARID3B
CUI: C0008924
Disease:
Cleft upper lip 		0.700 GeneticVariation GWASCAT Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate. 28054174 2017
dbSNP: rs11072494
rs11072494
Entrez Id: 10620
Gene Symbol: ARID3B
ARID3B
CUI: C0008925
Disease:
Cleft Palate 		0.700 GeneticVariation GWASCAT Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate. 28054174 2017
dbSNP: rs74781061
rs74781061
Entrez Id: 10620
Gene Symbol: ARID3B
ARID3B
CUI: C0014175
Disease:
Endometriosis 		G 0.700 GeneticVariation GWASCAT New variants near RHOJ and C2, HLA-DRA region and susceptibility to endometriosis in the Polish population-The genome-wide association study. 28881265 2017
dbSNP: rs10459648
rs10459648
Entrez Id: 10620
Gene Symbol: ARID3B
ARID3B
CUI: C0265240
Disease:
Goldenhar Syndrome 		T 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia. 26853712 2016
dbSNP: rs8041357
rs8041357
Entrez Id: 10620
Gene Symbol: ARID3B
ARID3B
CUI: C0699885
Disease:
Carcinoma of bladder 		0.010 GeneticVariation BEFREE SNP rs8041357, which is in complete linkage disequilibrium (r(2) = 1) with rs11543198, was also associated with bladder cancer risk in Europeans (P = 0.045 for an additive and P = 0.025 for a recessive model), despite much lower minor allele frequency in Europeans (3.7%) compared with the Japanese (22.2%). 25281661 2015
dbSNP: rs8041357
rs8041357
Entrez Id: 10620
Gene Symbol: ARID3B
ARID3B
CUI: C0005684
Disease:
Malignant neoplasm of urinary bladder 		0.010 GeneticVariation BEFREE SNP rs8041357, which is in complete linkage disequilibrium (r(2) = 1) with rs11543198, was also associated with bladder cancer risk in Europeans (P = 0.045 for an additive and P = 0.025 for a recessive model), despite much lower minor allele frequency in Europeans (3.7%) compared with the Japanese (22.2%). 25281661 2015
dbSNP: rs8041357
rs8041357
Entrez Id: 10620
Gene Symbol: ARID3B
ARID3B
CUI: C0005695
Disease:
Bladder Neoplasm 		0.010 GeneticVariation BEFREE SNP rs8041357, which is in complete linkage disequilibrium (r(2) = 1) with rs11543198, was also associated with bladder cancer risk in Europeans (P = 0.045 for an additive and P = 0.025 for a recessive model), despite much lower minor allele frequency in Europeans (3.7%) compared with the Japanese (22.2%). 25281661 2015