ADAMTSL1, ADAMTS like 1, 92949

N. diseases: 40; N. variants: 16
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: rs2210327
rs2210327 		1.000 0.040 9 18109237 intron variant A/T snv 3.4E-02
CUI: C0018801
Disease: Heart failure
Heart failure 		Cardiovascular Diseases 0.800 1.000 1 2010 2010
dbSNP: rs7041139
rs7041139 		9 18013735 intron variant C/T snv 0.37
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 2 2019 2019
dbSNP: rs10511652
rs10511652 		1.000 0.040 9 18362867 intron variant A/G snv 0.54
CUI: C0027092
Disease: Myopia
Myopia 		Eye Diseases 0.700 1.000 1 2016 2016
dbSNP: rs10963676
rs10963676 		1.000 0.040 9 18622045 intron variant T/C;G snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 1 2006 2006
dbSNP: rs10963680
rs10963680 		9 18629285 intron variant G/A snv 0.23
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs114646018
rs114646018 		1.000 0.080 9 18890063 intron variant C/T snv 1.2E-02
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs11789653
rs11789653 		9 17993591 intron variant C/A;T snv
CUI: C1266708
Disease: Polybrominated biphenyl measurement
Polybrominated biphenyl measurement 		0.700 1.000 1 2017 2017
dbSNP: rs12006002
rs12006002 		1.000 0.080 9 18166901 intron variant C/T snv 0.30
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		Chemically-Induced Disorders; Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs146250839
rs146250839 		9 18189780 intron variant A/G snv 4.3E-03
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs146551666
rs146551666 		9 18645262 intron variant G/C snv 4.5E-02
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2019 2019
dbSNP: rs17185553
rs17185553 		1.000 0.080 9 17934122 intron variant G/C snv 6.5E-02
CUI: C0149925
Disease: Small cell carcinoma of lung
Small cell carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.700 1.000 1 2017 2017
dbSNP: rs7034696
rs7034696 		1.000 0.040 9 18804132 intron variant C/T snv 0.27
CUI: C0017601
Disease: Glaucoma
Glaucoma 		Eye Diseases 0.700 1.000 1 2011 2011
dbSNP: rs7041139
rs7041139 		9 18013735 intron variant C/T snv 0.37
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2019 2019
dbSNP: rs7862648
rs7862648 		9 18290859 intron variant A/G;T snv
CUI: C0038663
Disease: Suicide attempt
Suicide attempt 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs13299349
rs13299349 		1.000 0.120 9 18573362 mature miRNA variant G/A snv 0.32 0.27
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1755289
rs1755289 		1.000 0.080 9 17938353 intron variant T/C;G snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs551639398
rs551639398 		1.000 0.040 9 18636011 missense variant C/G snv 1.9E-04 5.6E-05
CUI: C0399526
Disease: Class III malocclusion
Class III malocclusion 		Stomatognathic Diseases 0.010 1.000 1 2019 2019