Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17024608
rs17024608
RBMS3
CUI: C3178777
Disease: Bisphosphonate-Associated Osteonecrosis of the Jaw
Bisphosphonate-Associated Osteonecrosis of the Jaw 		0.700 GeneticVariation GWASDB Association testing identified a significant marker in the RBMS3 gene, rs17024608 (p-value < 7 × 10(-8)); individuals positive for the SNP were 5.8× more likely to develop BRONJ (odds ratio, 5.8; 95% confidence interval, 3.1-11.1). 22267851

2012
dbSNP: rs4377455
rs4377455
RBMS3
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.700 GeneticVariation GWASDB A genome-wide association study of bipolar disorder in Norwegian individuals, followed by replication in Icelandic sample. 20451256

2010
dbSNP: rs9861037
rs9861037
RBMS3 ; LINC00693
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219

2012
dbSNP: rs9883185
rs9883185
RBMS3
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		0.700 GeneticVariation GWASDB Genome-wide association database developed in the Japanese Integrated Database Project. 19629137

2009