Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11157436
rs11157436
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: rs11157436
rs11157436
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
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: rs11157436
rs11157436
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
T 0.700 GeneticVariation GWASCAT Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study. 28447399

2017

dbSNP: rs11157436
rs11157436
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
T 0.700 GeneticVariation GWASCAT Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study. 28447399

2017

dbSNP: rs11157436
rs11157436
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
T 0.700 GeneticVariation GWASCAT Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study. 28447399

2017

dbSNP: rs11157436
rs11157436
CUI: C2363741
Disease: HIV-1 infection
HIV-1 infection
T 0.700 GeneticVariation GWASCAT Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study. 28447399

2017

dbSNP: rs11157436
rs11157436
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO
T 0.700 GeneticVariation GWASCAT Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study. 28447399

2017