Gene: ADAMTS17 ×
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: rs2573652
rs2573652
ADAMTS17 ; LOC105371022
1 15 99974409 missense variant T/C;G snv 0.66; 4.0E-06 0.700 1.000 2 2015 2019
dbSNP: rs72755233
rs72755233
ADAMTS17
5 1.000 0.080 15 100152748 missense variant G/A;T snv 7.1E-02; 3.2E-05 0.700 1.000 2 2017 2019
dbSNP: rs145482150
rs145482150
ADAMTS17
1 15 99993107 missense variant C/T snv 2.0E-04 2.0E-04 0.700 1.000 1 2019 2019
dbSNP: rs149578709
rs149578709
ADAMTS17
1 15 100132203 intron variant A/G snv 9.0E-03 5.2E-03 0.700 1.000 1 2019 2019
dbSNP: rs2573625
rs2573625
ADAMTS17
1 15 99972953 3 prime UTR variant C/T snv 0.62 0.700 1.000 1 2014 2014
dbSNP: rs2581348
rs2581348
ADAMTS17
1 15 99973858 3 prime UTR variant C/T snv 0.63 0.700 1.000 1 2019 2019
dbSNP: rs2727195
rs2727195
ADAMTS17
1 15 99972912 3 prime UTR variant G/A snv 0.61 0.700 1.000 1 2019 2019
dbSNP: rs28411867
rs28411867
ADAMTS17
1 15 100314288 intron variant C/T snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs397807524
rs397807524
ADAMTS17
1 15 100052239 intron variant -/AA ins 7.0E-06 0.700 1.000 1 2019 2019
dbSNP: rs4369638
rs4369638
ADAMTS17
1 15 100254158 synonymous variant C/T snv 0.75 0.76 0.700 1.000 1 2019 2019
dbSNP: rs4467054
rs4467054
ADAMTS17
1 15 100255167 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs4533267
rs4533267
ADAMTS17
2 15 100246066 intron variant A/G snv 0.63 0.700 1.000 1 2008 2008
dbSNP: rs4965593
rs4965593
ADAMTS17
2 15 100218180 intron variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs4965598
rs4965598
ADAMTS17
2 15 100219409 intron variant C/A;T snv 0.700 1.000 1 2010 2010
dbSNP: rs4965612
rs4965612
ADAMTS17
1 15 100261237 intron variant A/G snv 0.72 0.700 1.000 1 2017 2017
dbSNP: rs76301628
rs76301628
ADAMTS17
1 15 100183232 intron variant G/T snv 3.4E-02 0.700 1.000 1 2019 2019