ADAMTSL3, ADAMTS like 3, 57188

N. diseases: 35; N. variants: 31
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: rs181914721
rs181914721 		1.000 0.040 15 83819856 missense variant G/A snv 3.7E-04 1.2E-04
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs7175718
rs7175718 		0.882 0.120 15 83900350 intron variant A/C snv 1.6E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs7175718
rs7175718 		0.882 0.120 15 83900350 intron variant A/C snv 1.6E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs950169
rs950169 		1.000 0.040 15 84037709 missense variant C/T snv 0.22 0.19
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.800 1.000 5 2009 2019
dbSNP: rs10906982
rs10906982 		15 83899406 intron variant T/A snv 0.63
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2008 2019
dbSNP: rs4842838
rs4842838 		15 83913372 missense variant G/A;T snv 1.6E-05; 0.61
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2009 2019
dbSNP: rs11259933
rs11259933 		15 83911404 intron variant G/A snv 0.63
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2013 2019
dbSNP: rs11259936
rs11259936 		15 83911830 intron variant A/C;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2010 2019
dbSNP: rs2401171
rs2401171 		15 83888924 intron variant T/G snv 0.62
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2015 2019
dbSNP: rs7183263
rs7183263 		15 83904289 intron variant T/G snv 0.63
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2010 2019
dbSNP: rs10152300
rs10152300 		1.000 0.040 15 83724155 intron variant G/A snv 0.84
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.700 1.000 1 2019 2019
dbSNP: rs111470917
rs111470917 		15 83916786 intron variant -/TAAA delins
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs11630762
rs11630762 		15 83946227 intron variant G/C snv 0.30
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs118136305
rs118136305 		15 83769541 intron variant T/C;G snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs11856122
rs11856122 		15 83907596 intron variant G/A snv 0.63
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution 		0.700 1.000 1 2019 2019
dbSNP: rs2135880
rs2135880 		15 83920861 intron variant T/G snv 0.63
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4523894
rs4523894 		1.000 0.040 15 83847191 intron variant C/G snv 7.0E-02
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.700 1.000 1 2019 2019
dbSNP: rs7170165
rs7170165 		15 83878087 intron variant A/C;G snv
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases 		Respiratory Tract Diseases 0.700 1.000 1 2019 2019
dbSNP: rs8031704
rs8031704 		15 83982433 synonymous variant C/A;T snv 0.33; 8.0E-06
CUI: C0518026
Disease: body fat percentage (physical finding)
body fat percentage (physical finding) 		0.700 1.000 1 2019 2019
dbSNP: rs8038454
rs8038454 		15 83670684 intron variant G/A;C;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs906427
rs906427 		15 83978455 intron variant T/A;C snv
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019