Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs140147
rs140147
Entrez Id: 84164
Gene Symbol: ASCC2
ASCC2
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis
0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs140147
rs140147
Entrez Id: 84164
Gene Symbol: ASCC2
ASCC2
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs28265
rs28265
Entrez Id: 84164
Gene Symbol: ASCC2
ASCC2
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
C 0.700 GeneticVariation GWASCAT Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. 29632382 2018
dbSNP: rs9608816
rs9608816
Entrez Id: 84164
Gene Symbol: ASCC2
ASCC2
CUI: C0005586
Disease:
Bipolar Disorder
0.700 GeneticVariation GWASCAT Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis. 27890468 2017
dbSNP: rs9608816
rs9608816
Entrez Id: 84164
Gene Symbol: ASCC2
ASCC2
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder
0.700 GeneticVariation GWASCAT Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis. 27890468 2017
dbSNP: rs249394
rs249394
Entrez Id: 84164
Gene Symbol: ASCC2
ASCC2
CUI: C0206161
Disease:
Reticulocyte count (procedure)
C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016