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: rs2681492
rs2681492
10 0.925 0.040 12 89619312 intron variant T/C;G snv 0.710 1.000 2 2013 2018
dbSNP: rs429358
rs429358
66 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.710 1.000 2 2019 2019
dbSNP: rs403814
rs403814
1 18 6282594 intron variant A/C snv 0.27 0.710 1.000 1 2016 2016
dbSNP: rs786205050
rs786205050
7 0.827 0.080 16 1212024 missense variant A/G snv 7.0E-06 0.710 1.000 1 2016 2016
dbSNP: rs9791170
rs9791170
1 5 132233934 intron variant T/C snv 0.59 0.710 1.000 1 2009 2009
dbSNP: rs1565930588
rs1565930588
19 0.882 0.160 12 119193787 frameshift variant TACTCAACATTTGG/- del 0.700 1.000 3 2016 2018
dbSNP: rs167479
rs167479
5 19 11416089 missense variant T/A;C;G snv 0.700 1.000 2 2016 2016
dbSNP: rs1902859
rs1902859
4 4 80236549 regulatory region variant T/C snv 0.27 0.700 1.000 2 2015 2018
dbSNP: rs28933386
rs28933386
15 0.752 0.400 12 112477719 missense variant A/G snv 1.2E-05 7.0E-06 0.700 1.000 2 2001 2006
dbSNP: rs4409766
rs4409766
6 1.000 0.040 10 102856906 intron variant T/C snv 0.14 0.700 1.000 2 2015 2018
dbSNP: rs6969780
rs6969780
4 7 27119517 splice region variant G/A;C snv 0.700 1.000 2 2016 2017
dbSNP: rs7302981
rs7302981
4 12 50144032 missense variant A/G;T snv 0.69 0.71 0.700 1.000 2 2016 2016
dbSNP: rs880315
rs880315
9 0.925 0.120 1 10736809 intron variant T/C snv 0.32 0.700 1.000 2 2015 2018
dbSNP: rs10033366
rs10033366
1 4 110409934 intron variant T/C snv 0.92 0.700 1.000 1 2018 2018
dbSNP: rs10069554
rs10069554
1 5 33204354 intron variant T/C snv 0.45 0.700 1.000 1 2018 2018
dbSNP: rs10184428
rs10184428
5 2 164155317 intron variant C/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs10188442
rs10188442
1 2 132431666 intron variant C/T snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs1027989
rs1027989
LYN
3 8 55901862 intron variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs10279895
rs10279895
1 7 27288591 intergenic variant A/G snv 2.9E-02 0.700 1.000 1 2017 2017
dbSNP: rs10496288
rs10496288
1 2 83065441 intergenic variant T/C snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs10496289
rs10496289
1 2 83066256 intergenic variant C/T snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs10745332
rs10745332
3 1 112646431 intron variant G/A snv 0.77 0.700 1.000 1 2015 2015
dbSNP: rs10776752
rs10776752
4 1 112501706 intron variant G/T snv 8.8E-02 0.700 1.000 1 2018 2018
dbSNP: rs10785581
rs10785581
1 12 45537190 intron variant C/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs10857147
rs10857147
9 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 0.700 1.000 1 2018 2018