Gene: ASCC2
Alternate names for this Gene:
ASC1p100|p100
Gene Summary:
Gene is located in Chromosome:
22
Location in Chromosome :
22q12.2
Description of this Gene:
activating signal cointegrator 1 complex subunit 2
Type of Gene:
protein-coding
rs140147
in
ASCC2
gene and
Adolescent idiopathic scoliosis
PMID 30019117
2018 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.
rs9608816
in
ASCC2
gene and
Attention deficit hyperactivity disorder
PMID 27890468
2017 Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis.
rs9608816
in
ASCC2
gene and
Bipolar Disorder
PMID 27890468
2017 Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis.
rs28265
in
ASCC2
gene and
Diabetes Mellitus, Non-Insulin-Dependent
PMID 29632382
2018 Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.
rs249394
in
ASCC2
gene and
Reticulocyte count (procedure)
PMID 27863252
2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
rs140147
in
ASCC2
gene and
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
PMID 30019117
2018 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.