Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11075747
rs11075747
Entrez Id: 11060
Gene Symbol: WWP2
WWP2
CUI: C0023508
Disease:
White Blood Cell Count procedure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12926791
rs12926791
Entrez Id: 11060
Gene Symbol: WWP2
WWP2
CUI: C1314691
Disease:
Age at menarche
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2173714
rs2173714
Entrez Id: 11060
Gene Symbol: WWP2
WWP2
CUI: C0200638
Disease:
Eosinophil count procedure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs3790076
rs3790076
Entrez Id: 11060
Gene Symbol: WWP2
WWP2
CUI: C0042834
Disease:
Vital capacity
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs4146819
rs4146819
Entrez Id: 11060
Gene Symbol: WWP2
WWP2
CUI: C0205682
Disease:
Waist-Hip Ratio
A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs4985445
rs4985445
Entrez Id: 11060
Gene Symbol: WWP2
WWP2
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs56140069
rs56140069
Entrez Id: 11060
Gene Symbol: WWP2
WWP2
CUI: C0017654
Disease:
Glomerular Filtration Rate
A 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs62050038
rs62050038
Entrez Id: 11060
Gene Symbol: WWP2
WWP2
CUI: C0017654
Disease:
Glomerular Filtration Rate
A 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs6499255
rs6499255
Entrez Id: 11060
Gene Symbol: WWP2
WWP2
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs77870048
rs77870048
Entrez Id: 11060;406932
Gene Symbol: WWP2;MIR140
WWP2;MIR140
CUI: C0871470
Disease:
Systolic Pressure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs77870048
rs77870048
Entrez Id: 11060;406932
Gene Symbol: WWP2;MIR140
WWP2;MIR140
CUI: C0428883
Disease:
Diastolic blood pressure
T 0.700 GeneticVariation GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019
dbSNP: rs8047194
rs8047194
Entrez Id: 11060
Gene Symbol: WWP2
WWP2
CUI: C0042834
Disease:
Vital capacity
T 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs8047194
rs8047194
Entrez Id: 11060
Gene Symbol: WWP2
WWP2
CUI: C0016529
Disease:
Forced expiratory volume function
T 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs8057620
rs8057620
Entrez Id: 11060
Gene Symbol: WWP2
WWP2
CUI: C0424621
Disease:
Body Fat Distribution
T 0.700 GeneticVariation GWASCAT Genome-wide association study of body fat distribution identifies adiposity loci and sex-specific genetic effects. 30664634 2019
dbSNP: rs148604553
rs148604553
Entrez Id: 11060
Gene Symbol: WWP2
WWP2
CUI: C2985280
Disease:
Blood Protein Measurement
TAC 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs151186597
rs151186597
Entrez Id: 11060
Gene Symbol: WWP2
WWP2
CUI: C0596887
Disease:
mathematical ability
T 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs2173714
rs2173714
Entrez Id: 11060
Gene Symbol: WWP2
WWP2
CUI: C0021704
Disease:
Intelligence
0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs2937124
rs2937124
Entrez Id: 11060
Gene Symbol: WWP2
WWP2
CUI: C0202236
Disease:
Triglycerides measurement
T 0.700 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018
dbSNP: rs34195470
rs34195470
Entrez Id: 11060
Gene Symbol: WWP2
WWP2
CUI: C0409959
Disease:
Osteoarthritis, Knee
G 0.700 GeneticVariation GWASCAT Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis. 30374069 2018
dbSNP: rs62051384
rs62051384
Entrez Id: 11060
Gene Symbol: WWP2
WWP2
CUI: C0158360
Disease:
Fibromatosis, Plantar
T 0.700 GeneticVariation GWASCAT Two Genetic Variants Associated with Plantar Fascial Disorders. 29534260 2018
dbSNP: rs62051384
rs62051384
Entrez Id: 11060
Gene Symbol: WWP2
WWP2
CUI: C0149756
Disease:
Fasciitis, Plantar
T 0.700 GeneticVariation GWASCAT Two Genetic Variants Associated with Plantar Fascial Disorders. 29534260 2018
dbSNP: rs56117028
rs56117028
Entrez Id: 11060
Gene Symbol: WWP2
WWP2
CUI: C0016529
Disease:
Forced expiratory volume function
A 0.700 GeneticVariation GWASCAT Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank. 26423011 2015
dbSNP: rs7205289
rs7205289
Entrez Id: 11060;406932
Gene Symbol: WWP2;MIR140
WWP2;MIR140
CUI: C2981150
Disease:
Uranostaphyloschisis
0.010 GeneticVariation BEFREE We concluded that infants with CA/AA genotypes at rs7205289 and maternal passive smoking during the first trimester may synergistically contribute to cleft palate risk by decreasing microRNA-140 during palatal development. 22012839 2011
dbSNP: rs7205289
rs7205289
Entrez Id: 11060;406932
Gene Symbol: WWP2;MIR140
WWP2;MIR140
CUI: C1837218
Disease:
Cleft palate, isolated
0.010 GeneticVariation BEFREE We concluded that infants with CA/AA genotypes at rs7205289 and maternal passive smoking during the first trimester may synergistically contribute to cleft palate risk by decreasing microRNA-140 during palatal development. 22012839 2011
dbSNP: rs7205289
rs7205289
Entrez Id: 11060;406932
Gene Symbol: WWP2;MIR140
WWP2;MIR140
CUI: C0008925
Disease:
Cleft Palate
0.010 GeneticVariation BEFREE We concluded that infants with CA/AA genotypes at rs7205289 and maternal passive smoking during the first trimester may synergistically contribute to cleft palate risk by decreasing microRNA-140 during palatal development. 22012839 2011