Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs892085
rs892085
Entrez Id: 81890
Gene Symbol: QTRT1
QTRT1
CUI: C0033860
Disease:
Psoriasis 		A 0.800 GeneticVariation GWASCAT Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms. 25574825 2015
dbSNP: rs892085
rs892085
Entrez Id: 81890
Gene Symbol: QTRT1
QTRT1
CUI: C0033860
Disease:
Psoriasis 		0.800 GeneticVariation GWASDB Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. 23143594 2012
dbSNP: rs892085
rs892085
Entrez Id: 81890
Gene Symbol: QTRT1
QTRT1
CUI: C0033860
Disease:
Psoriasis 		A 0.800 GeneticVariation GWASCAT Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. 23143594 2012
dbSNP: rs11085744
rs11085744
Entrez Id: 81890
Gene Symbol: QTRT1
QTRT1
CUI: C0205682
Disease:
Waist-Hip Ratio 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11085744
rs11085744
Entrez Id: 81890
Gene Symbol: QTRT1
QTRT1
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: rs892085
rs892085
Entrez Id: 81890
Gene Symbol: QTRT1
QTRT1
CUI: C0263361
Disease:
Psoriasis vulgaris 		A 0.700 GeneticVariation GWASCAT Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture. 26626624 2015
dbSNP: rs9807841
rs9807841
Entrez Id: 81890
Gene Symbol: QTRT1
QTRT1
CUI: C0033860
Disease:
Psoriasis 		0.700 GeneticVariation GWASCAT Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms. 25574825 2015
dbSNP: rs751857027
rs751857027
Entrez Id: 81890
Gene Symbol: QTRT1
QTRT1
CUI: C0085390
Disease:
Li-Fraumeni Syndrome 		0.010 GeneticVariation BEFREE Selective acquisition of IDH1 R132C mutations in astrocytomas associated with Li-Fraumeni syndrome. 19340432 2009
dbSNP: rs751857027
rs751857027
Entrez Id: 81890
Gene Symbol: QTRT1
QTRT1
CUI: C0004114
Disease:
Astrocytoma 		0.010 GeneticVariation BEFREE Without exception, all were R132C (CGT-->TGT), which in sporadic astrocytomas accounts for <5% of IDH1 mutations. 19340432 2009
dbSNP: rs750966175
rs750966175
Entrez Id: 81890
Gene Symbol: QTRT1
QTRT1
CUI: C0027651
Disease:
Neoplasms 		0.010 GeneticVariation BEFREE Other three mutations were detected in three of five multiple tumors developed in the bilateral WT patient; a mutation of Delta45 in one of two tumors in the right kidney, and Ser45Cys (TCT --> TGT) and Ser45Pro (TCT --> CCT) in two of three tumors in the left kidney. 12239584 2002