TDRKH, tudor and KH domain containing, 11022

N. diseases: 9; N. variants: 5
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11810571
rs11810571 		1.000 0.040 1 151789832 intron variant C/A;G snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 2 2017 2018
dbSNP: rs11204885
rs11204885 		1.000 0.040 1 151775494 missense variant A/G;T snv 0.23 0.20
CUI: C4021107
Disease: Non-obstructive azoospermia
Non-obstructive azoospermia 		Male Urogenital Diseases 0.700 1.000 1 2011 2011
dbSNP: rs4845570
rs4845570 		1.000 0.040 1 151786628 intron variant C/T snv 0.79
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs541559418
rs541559418 		1.000 0.080 1 151788046 intron variant G/A;C snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs375454176
rs375454176 		1.000 0.040 1 151776497 missense variant C/T snv 1.2E-05 7.0E-06
CUI: C0393541
Disease: Distal Spinal Muscular Atrophy
Distal Spinal Muscular Atrophy 		Nervous System Diseases 0.700 0
dbSNP: rs375454176
rs375454176 		1.000 0.040 1 151776497 missense variant C/T snv 1.2E-05 7.0E-06
CUI: C2749625
Disease: Motor axonal neuropathy
Motor axonal neuropathy 		0.700 0