Gene: ADAMTSL3 ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs111470917
rs111470917
ADAMTSL3
1 15 83916786 intron variant -/TAAA delins 0.700 1.000 1 2019 2019
dbSNP: rs118136305
rs118136305
ADAMTSL3
1 15 83769541 intron variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs1383484
rs1383484
ADAMTSL3
2 15 83854003 intron variant C/T snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs2135880
rs2135880
ADAMTSL3
1 15 83920861 intron variant T/G snv 0.63 0.700 1.000 1 2019 2019
dbSNP: rs2585061
rs2585061
ADAMTSL3
1 15 83678999 intron variant A/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs7162542
rs7162542
ADAMTSL3
4 15 83845538 intron variant C/A;G;T snv 0.700 1.000 1 2014 2014
dbSNP: rs8024628
rs8024628
ADAMTSL3
1 15 83917711 intron variant A/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs8038454
rs8038454
ADAMTSL3
1 15 83670684 intron variant G/A;C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs950169
rs950169
ADAMTSL3
2 1.000 0.040 15 84037709 missense variant C/T snv 0.22 0.19 0.700 1.000 1 2017 2017
dbSNP: rs11259933
rs11259933
ADAMTSL3
2 15 83911404 intron variant G/A snv 0.63 0.700 1.000 2 2013 2019
dbSNP: rs11259936
rs11259936
ADAMTSL3
2 15 83911830 intron variant A/C;T snv 0.700 1.000 2 2010 2019
dbSNP: rs2401171
rs2401171
ADAMTSL3
1 15 83888924 intron variant T/G snv 0.62 0.700 1.000 2 2015 2019
dbSNP: rs7183263
rs7183263
ADAMTSL3
3 15 83904289 intron variant T/G snv 0.63 0.700 1.000 2 2010 2019
dbSNP: rs10906982
rs10906982
ADAMTSL3
2 15 83899406 intron variant T/A snv 0.63 0.700 1.000 3 2008 2019
dbSNP: rs4842838
rs4842838
ADAMTSL3
3 15 83913372 missense variant G/A;T snv 1.6E-05; 0.61 0.700 1.000 3 2009 2019