WNT5B, Wnt family member 5B, 81029

N. diseases: 39; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs35125553
rs35125553
Entrez Id: 81029;107984507
Gene Symbol: WNT5B;LOC107984507
WNT5B;LOC107984507
CUI: C0005938
Disease:
Bone Density
A 0.700 GeneticVariation GWASCAT Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects. 29304378 2018
dbSNP: rs10773971
rs10773971
Entrez Id: 81029
Gene Symbol: WNT5B
WNT5B
CUI: C0003868
Disease:
Arthritis, Gouty
0.700 GeneticVariation GWASCAT Gout and type 2 diabetes have a mutual inter-dependent effect on genetic risk factors and higher incidences. 22179738 2012
dbSNP: rs10773971
rs10773971
Entrez Id: 81029
Gene Symbol: WNT5B
WNT5B
CUI: C0018099
Disease:
Gout
0.700 GeneticVariation GWASCAT Gout and type 2 diabetes have a mutual inter-dependent effect on genetic risk factors and higher incidences. 22179738 2012
dbSNP: rs2887571
rs2887571
Entrez Id: 81029;107984507
Gene Symbol: WNT5B;LOC107984507
WNT5B;LOC107984507
CUI: C0177804
Disease:
Bone Mineral Density Test
A 0.700 GeneticVariation GWASDB Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. 22504420 2012
dbSNP: rs2887571
rs2887571
Entrez Id: 81029;107984507
Gene Symbol: WNT5B;LOC107984507
WNT5B;LOC107984507
CUI: C0005938
Disease:
Bone Density
A 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. 22504420 2012
dbSNP: rs4766398
rs4766398
Entrez Id: 81029
Gene Symbol: WNT5B
WNT5B
CUI: C0003868
Disease:
Arthritis, Gouty
0.700 GeneticVariation GWASCAT Gout and type 2 diabetes have a mutual inter-dependent effect on genetic risk factors and higher incidences. 22179738 2012
dbSNP: rs4766398
rs4766398
Entrez Id: 81029
Gene Symbol: WNT5B
WNT5B
CUI: C0018099
Disease:
Gout
0.700 GeneticVariation GWASCAT Gout and type 2 diabetes have a mutual inter-dependent effect on genetic risk factors and higher incidences. 22179738 2012
dbSNP: rs735890
rs735890
Entrez Id: 81029
Gene Symbol: WNT5B
WNT5B
CUI: C0029456
Disease:
Osteoporosis
0.010 GeneticVariation BEFREE This study is the first evidence of the association of WNT5b rs735890, and c.[1406A; 3132C] and c.[1406G; 3132C] haplotypes of SFRP1 with BMD variation in osteoporosis, probably by altering microRNA target sites, in elderly persons. 30055306 2018
dbSNP: rs2270031
rs2270031
Entrez Id: 81029
Gene Symbol: WNT5B
WNT5B
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE Two thousand seven hundred and one Caucasian middle-aged men from the prospective Northwick Park Heart Study II (NPHSII) of whom 153 developed T2D over 15 years and 1268 Caucasian middle-aged patients with T2D (60% male) were genotyped using a TaqMan assay for the IVS3C>G variant (rs2270031) in the WNT5B gene. 18555673 2009