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: 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: rs10906982
rs10906982
15 83899406 intron variant T/A snv 0.63
CUI: C0489786
Disease: Height
Height
0.700 1.000 2 2008 2010
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: 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: 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: rs11259933
rs11259933
15 83911404 intron variant G/A snv 0.63
CUI: C0489786
Disease: Height
Height
0.700 1.000 1 2013 2013
dbSNP: rs11259936
rs11259936
15 83911830 intron variant A/C;T snv
CUI: C0489786
Disease: Height
Height
0.700 1.000 1 2010 2010
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: 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: 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: 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: 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: 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: 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