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: rs7162542
rs7162542 		15 83845538 intron variant C/A;G;T snv
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		Behavior and Behavior Mechanisms 0.700 1.000 1 2017 2017
dbSNP: rs7162542
rs7162542 		15 83845538 intron variant C/A;G;T snv
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2017 2017
dbSNP: rs7162542
rs7162542 		15 83845538 intron variant C/A;G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2014 2014
dbSNP: rs7162542
rs7162542 		15 83845538 intron variant C/A;G;T snv
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
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: 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: C0027404
Disease: Narcolepsy
Narcolepsy 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2009 2009
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: rs7183263
rs7183263 		15 83904289 intron variant T/G snv 0.63
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs7183263
rs7183263 		15 83904289 intron variant T/G snv 0.63
CUI: C0562350
Disease: Hip circumference
Hip circumference 		0.700 1.000 1 2015 2015
dbSNP: rs8024628
rs8024628 		15 83917711 intron variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs8030379
rs8030379 		15 83922158 intron variant G/A snv 0.63
CUI: C0455829
Disease: Waist Circumference
Waist Circumference 		0.700 1.000 1 2016 2016
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
dbSNP: rs950169
rs950169 		1.000 0.040 15 84037709 missense variant C/T snv 0.22 0.19
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs142860011
rs142860011 		1.000 0.080 15 83913151 missense variant G/A snv 1.6E-05 1.4E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs1439091253
rs1439091253 		1.000 0.080 15 83885128 missense variant G/A snv 4.0E-06 7.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs146769560
rs146769560 		1.000 0.080 15 83970556 missense variant C/T snv 2.8E-05 2.1E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs181914721
rs181914721 		1.000 0.040 15 83819856 missense variant G/A snv 3.7E-04 1.2E-04
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.010 1.000 1 2018 2018
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