SDK2, sidekick cell adhesion molecule 2, 54549

N. diseases: 8; N. variants: 2
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.100 GeneticVariation disease GWASCAT A new 3p25 locus is associated with liver fibrosis progression in human immunodeficiency virus/hepatitis C virus-coinfected patients. 27339598 2016
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.100 GeneticVariation disease GWASCAT A new 3p25 locus is associated with liver fibrosis progression in human immunodeficiency virus/hepatitis C virus-coinfected patients. 27339598 2016
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
0.100 GeneticVariation phenotype GWASCAT A new 3p25 locus is associated with liver fibrosis progression in human immunodeficiency virus/hepatitis C virus-coinfected patients. 27339598 2016
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
0.100 GeneticVariation phenotype GWASCAT A new 3p25 locus is associated with liver fibrosis progression in human immunodeficiency virus/hepatitis C virus-coinfected patients. 27339598 2016
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO
0.100 GeneticVariation phenotype GWASCAT A new 3p25 locus is associated with liver fibrosis progression in human immunodeficiency virus/hepatitis C virus-coinfected patients. 27339598 2016
CUI: C2363741
Disease: HIV-1 infection
HIV-1 infection
0.100 GeneticVariation disease GWASCAT A new 3p25 locus is associated with liver fibrosis progression in human immunodeficiency virus/hepatitis C virus-coinfected patients. 27339598 2016
CUI: C0030319
Disease: Panic Disorder
Panic Disorder
0.100 GeneticVariation disease GWASDB Genome-wide association study of panic disorder in the Japanese population. 19165232 2009
CUI: C0030319
Disease: Panic Disorder
Panic Disorder
0.100 GeneticVariation disease GWASCAT Genome-wide association study of panic disorder in the Japanese population. 19165232 2009
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease
0.010 GeneticVariation disease BEFREE We identified three variants suggestively associated with HT: rs12944194 located 206 kb from SDK2 (P = 1.8 × 10<sup>-6</sup>), rs75201096 inside GNA14 (P = 2.41 × 10<sup>-5</sup>) and rs791903 inside IP6K3 (P = 3.16 × 10<sup>-5</sup>). 30284222 2019