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: 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: 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: 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: 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: rs111470917
rs111470917 		15 83916786 intron variant -/TAAA delins
CUI: C0005890
Disease: Body Height
Body Height 		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: rs1383484
rs1383484 		15 83854003 intron variant C/T snv 0.32
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2011 2011
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: rs2585061
rs2585061 		15 83678999 intron variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		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: 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: 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: 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: 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: 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: 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