RUNDC3B, RUN domain containing 3B, 154661

N. diseases: 10; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6966166
rs6966166
Entrez Id: 154661
Gene Symbol: RUNDC3B
RUNDC3B
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs10264856
rs10264856
Entrez Id: 5243;154661
Gene Symbol: ABCB1;RUNDC3B
ABCB1;RUNDC3B
CUI: C1314691
Disease:
Age at menarche 		0.700 GeneticVariation GWASCAT Bivariate Genome-Wide Association Study Implicates ATP6V1G1 as a Novel Pleiotropic Locus Underlying Osteoporosis and Age at Menarche. 26312577 2015
dbSNP: rs114137957
rs114137957
Entrez Id: 154661
Gene Symbol: RUNDC3B
RUNDC3B
CUI: C0429087
Disease:
Electrocardiogram: P-R interval 		0.700 GeneticVariation GWASCAT Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects. 24324551 2013
dbSNP: rs3747802
rs3747802
Entrez Id: 5243;154661
Gene Symbol: ABCB1;RUNDC3B
ABCB1;RUNDC3B
CUI: C0036341
Disease:
Schizophrenia 		0.010 GeneticVariation BEFREE In this study, we investigated whether 9 SNPs in ABCB1 (rs6946119, rs28401781, rs4148739, and rs3747802), ABCB6 (rs1109866, rs1109867, rs3731885, and rs3755047), and ABCG1 (rs182694) contribute to the risk of SCZ in a Han Chinese population. 31189171 2019