TDRKH, tudor and KH domain containing, 11022

N. diseases: 9; N. variants: 5
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs541559418
rs541559418
Entrez Id: 11022
Gene Symbol: TDRKH
TDRKH
CUI: C0004096
Disease:
Asthma 		A 0.700 GeneticVariation GWASCAT Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct. 30929738 2019
dbSNP: rs11810571
rs11810571
Entrez Id: 11022;109729141
Gene Symbol: TDRKH;TDRKH-AS1
TDRKH;TDRKH-AS1
CUI: C1956346
Disease:
Coronary Artery Disease 		C 0.700 GeneticVariation GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778 2018
dbSNP: rs4845570
rs4845570
Entrez Id: 11022
Gene Symbol: TDRKH
TDRKH
CUI: C1956346
Disease:
Coronary Artery Disease 		T 0.700 GeneticVariation GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778 2018
dbSNP: rs11810571
rs11810571
Entrez Id: 11022;109729141
Gene Symbol: TDRKH;TDRKH-AS1
TDRKH;TDRKH-AS1
CUI: C1956346
Disease:
Coronary Artery Disease 		G 0.700 GeneticVariation GWASCAT Association analyses based on false discovery rate implicate new loci for coronary artery disease. 28714975 2017
dbSNP: rs11204885
rs11204885
Entrez Id: 11022
Gene Symbol: TDRKH
TDRKH
CUI: C4021107
Disease:
Non-obstructive azoospermia 		0.700 GeneticVariation GWASDB A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia. 22197933 2011
dbSNP: rs375454176
rs375454176
Entrez Id: 11022
Gene Symbol: TDRKH
TDRKH
CUI: C2749625
Disease:
Motor axonal neuropathy 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs375454176
rs375454176
Entrez Id: 11022
Gene Symbol: TDRKH
TDRKH
CUI: C0393541
Disease:
Distal Spinal Muscular Atrophy 		T 0.700 GeneticVariation CLINVAR