WAPL, WAPL cohesin release factor, 23063

N. diseases: 8; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3858281
rs3858281
Entrez Id: 23063
Gene Symbol: WAPL
WAPL
CUI: C0596887
Disease:
mathematical ability 		G 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: rs3858281
rs3858281
Entrez Id: 23063
Gene Symbol: WAPL
WAPL
CUI: C0596887
Disease:
mathematical ability 		A 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: rs182554582
rs182554582
Entrez Id: 23063
Gene Symbol: WAPL
WAPL
CUI: C3548479
Disease:
response to bronchodilator 		A 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs182554582
rs182554582
Entrez Id: 23063
Gene Symbol: WAPL
WAPL
CUI: C0016529
Disease:
Forced expiratory volume function 		A 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs7075426
rs7075426
Entrez Id: 23063
Gene Symbol: WAPL
WAPL
CUI: C0149931
Disease:
Migraine Disorders 		A 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis identifies new susceptibility loci for migraine. 23793025 2013
dbSNP: rs7075426
rs7075426
Entrez Id: 23063
Gene Symbol: WAPL
WAPL
CUI: C0338480
Disease:
Common Migraine 		A 0.700 GeneticVariation GWASDB Genome-wide meta-analysis identifies new susceptibility loci for migraine. 23793025 2013
dbSNP: rs1471281484
rs1471281484
Entrez Id: 23063
Gene Symbol: WAPL
WAPL
CUI: C0025362
Disease:
Mental Retardation 		0.010 GeneticVariation BEFREE Five individuals carry a <i>STAG2</i> p.Ser327Asn (c.980 G > A) variant that perfectly cosegregates with a phenotype of syndromic mental retardation in a characteristic X-linked recessive pattern. 29263825 2017
dbSNP: rs1471281484
rs1471281484
Entrez Id: 23063
Gene Symbol: WAPL
WAPL
CUI: C3714756
Disease:
Intellectual Disability 		0.010 GeneticVariation BEFREE Five individuals carry a <i>STAG2</i> p.Ser327Asn (c.980 G > A) variant that perfectly cosegregates with a phenotype of syndromic mental retardation in a characteristic X-linked recessive pattern. 29263825 2017
dbSNP: rs11202058
rs11202058
Entrez Id: 23063
Gene Symbol: WAPL
WAPL
CUI: C0302592
Disease:
Cervix carcinoma 		0.010 GeneticVariation BEFREE Rs7083506 and rs11202058 polymorphisms of hWAPL and their haplotype T-A were associated with cervical cancer. 26722608 2015
dbSNP: rs11202058
rs11202058
Entrez Id: 23063
Gene Symbol: WAPL
WAPL
CUI: C4048328
Disease:
cervical cancer 		0.010 GeneticVariation BEFREE Rs7083506 and rs11202058 polymorphisms of hWAPL and their haplotype T-A were associated with cervical cancer. 26722608 2015
dbSNP: rs11202058
rs11202058
Entrez Id: 23063
Gene Symbol: WAPL
WAPL
CUI: C0007847
Disease:
Malignant tumor of cervix 		0.010 GeneticVariation BEFREE Rs7083506 and rs11202058 polymorphisms of hWAPL and their haplotype T-A were associated with cervical cancer. 26722608 2015
dbSNP: rs7083506
rs7083506
Entrez Id: 23063
Gene Symbol: WAPL
WAPL
CUI: C4048328
Disease:
cervical cancer 		0.010 GeneticVariation BEFREE TT genotype of rs7083506 increased the susceptibility of cervical cancer in TT vs. CC model and TT vs. CT+TT model (OR=2.249, 95% CI=1.018-4.970; OR=2.287, 95% CI=1.069-4.896). 26722608 2015
dbSNP: rs7083506
rs7083506
Entrez Id: 23063
Gene Symbol: WAPL
WAPL
CUI: C0007847
Disease:
Malignant tumor of cervix 		0.010 GeneticVariation BEFREE TT genotype of rs7083506 increased the susceptibility of cervical cancer in TT vs. CC model and TT vs. CT+TT model (OR=2.249, 95% CI=1.018-4.970; OR=2.287, 95% CI=1.069-4.896). 26722608 2015
dbSNP: rs7083506
rs7083506
Entrez Id: 23063
Gene Symbol: WAPL
WAPL
CUI: C0302592
Disease:
Cervix carcinoma 		0.010 GeneticVariation BEFREE TT genotype of rs7083506 increased the susceptibility of cervical cancer in TT vs. CC model and TT vs. CT+TT model (OR=2.249, 95% CI=1.018-4.970; OR=2.287, 95% CI=1.069-4.896). 26722608 2015