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: rs2251219
rs2251219
14 0.732 0.120 3 52550771 synonymous variant T/C;G snv 0.39; 4.0E-06 0.34 0.810 1.000 1 2010 2010
dbSNP: rs10020288
rs10020288
2 1.000 0.040 4 28686220 intergenic variant G/A snv 0.38 0.700 1.000 1 2018 2018
dbSNP: rs10144845
rs10144845
2 1.000 0.040 14 74771067 intron variant C/T snv 0.62 0.700 1.000 1 2018 2018
dbSNP: rs10156548
rs10156548
2 1.000 0.040 9 23318435 intron variant G/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10405382
rs10405382
2 1.000 0.040 19 32405810 5 prime UTR variant C/G snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs10429537
rs10429537
2 1.000 0.040 9 23346844 intron variant C/G snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs1055447
rs1055447
2 1.000 0.040 11 47164873 3 prime UTR variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10891564
rs10891564
2 1.000 0.040 11 113503291 intergenic variant G/A snv 0.34 0.700 1.000 1 2018 2018
dbSNP: rs10950393
rs10950393
2 1.000 0.040 7 12223920 intron variant T/C snv 0.50 0.700 1.000 1 2018 2018
dbSNP: rs10965780
rs10965780
3 1.000 0.040 9 23341717 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs11039149
rs11039149
6 0.827 0.280 11 47255124 intron variant A/G snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs11039409
rs11039409
2 1.000 0.040 11 47814169 intron variant A/C snv 0.22 0.700 1.000 1 2018 2018
dbSNP: rs111365677
rs111365677
3 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 0.700 1.000 1 2016 2016
dbSNP: rs11152363
rs11152363
2 1.000 0.040 18 55389957 intron variant G/A snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs11209175
rs11209175
2 1.000 0.040 1 67909145 intron variant C/T snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs112106319
rs112106319
3 0.925 0.040 9 115094539 intron variant A/T snv 2.8E-03 0.700 1.000 1 2016 2016
dbSNP: rs11214589
rs11214589
2 1.000 0.040 11 113374326 intron variant G/A snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs11214607
rs11214607
2 1.000 0.040 11 113441417 intron variant T/G snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs112538845
rs112538845
3 0.925 0.040 4 184084475 downstream gene variant C/T snv 1.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs113378111
rs113378111
3 1.000 0.040 2 9788024 intergenic variant G/A snv 2.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs114465512
rs114465512
3 1.000 0.040 22 22047895 intron variant C/T snv 4.7E-03 0.700 1.000 1 2016 2016
dbSNP: rs11514731
rs11514731
2 1.000 0.040 7 2011868 intron variant C/G snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs11599236
rs11599236
2 1.000 0.040 10 104694914 intron variant T/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs11605020
rs11605020
2 1.000 0.040 11 127110970 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs11608355
rs11608355
2 1.000 0.040 12 109441487 intron variant T/C snv 0.33 0.700 1.000 1 2018 2018