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: 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: rs2135551
rs2135551 		1.000 0.040 15 84039099 3 prime UTR variant A/G snv 0.19
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		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: C0027404
Disease: Narcolepsy
Narcolepsy 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs10906982
rs10906982 		15 83899406 intron variant T/A snv 0.63
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2008 2010
dbSNP: rs4842838
rs4842838 		15 83913372 missense variant G/A;T snv 1.6E-05; 0.61
CUI: C0489786
Disease: Height
Height 		0.700 1.000 2 2009 2010
dbSNP: rs11259936
rs11259936 		15 83911830 intron variant A/C;T snv
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: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs1383484
rs1383484 		15 83854003 intron variant C/T snv 0.32
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2011 2011
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: rs11259933
rs11259933 		15 83911404 intron variant G/A snv 0.63
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2013 2013
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: 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: 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: rs2030839
rs2030839 		15 83915207 intron variant T/C snv 0.63
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
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: rs4842838
rs4842838 		15 83913372 missense variant G/A;T snv 1.6E-05; 0.61
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs4842924
rs4842924 		15 83918855 intron variant C/T snv 0.63
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.700 1.000 1 2017 2017
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: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
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: 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: 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