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: 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