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: rs1452787
rs1452787
2 0.827 0.160 18 55539976 intron variant A/G snv 0.24 0.800 1.000 1 2013 2013
dbSNP: rs4676410
rs4676410
17 0.716 0.240 2 240624322 intron variant G/A snv 0.26 0.800 1.000 1 2013 2013
dbSNP: rs3197999
rs3197999
7 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 0.700 1.000 4 2011 2017
dbSNP: rs3184504
rs3184504
61 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.700 1.000 3 2013 2017
dbSNP: rs7426056
rs7426056
5 0.807 0.120 2 203747335 regulatory region variant A/G snv 0.81 0.700 1.000 3 2013 2017
dbSNP: rs11168249
rs11168249
8 0.807 0.120 12 47814585 intron variant T/C snv 0.50 0.700 1.000 2 2013 2016
dbSNP: rs13140464
rs13140464
1 0.925 0.040 4 122578590 regulatory region variant G/T snv 0.10 0.700 1.000 2 2013 2017
dbSNP: rs1788097
rs1788097
1 0.925 0.040 18 69876452 intron variant C/T snv 0.56 0.700 1.000 2 2013 2017
dbSNP: rs1893592
rs1893592
7 0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 0.700 1.000 2 2016 2017
dbSNP: rs2836883
rs2836883
3 0.882 0.080 21 39094818 intergenic variant G/A snv 0.23 0.700 1.000 2 2013 2017
dbSNP: rs3748816
rs3748816
2 0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 0.700 1.000 2 2013 2017
dbSNP: rs4147359
rs4147359
1 0.925 0.040 10 6066476 upstream gene variant G/A snv 0.33 0.700 1.000 2 2013 2017
dbSNP: rs56258221
rs56258221
1 0.925 0.040 6 90320722 intron variant T/C snv 0.13 0.700 1.000 2 2013 2017
dbSNP: rs60652743
rs60652743
1 0.925 0.040 19 46702450 intron variant A/G snv 0.16 0.700 1.000 2 2013 2017
dbSNP: rs7937682
rs7937682
1 0.925 0.040 11 111709215 intron variant G/A;C snv 0.700 1.000 2 2013 2017
dbSNP: rs1001007
rs1001007
5 0.827 0.120 3 46387167 intron variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1004234
rs1004234
5 0.827 0.120 5 132421409 intron variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10094579
rs10094579
5 0.807 0.280 8 89837077 downstream gene variant C/A snv 0.18 0.700 1.000 1 2016 2016
dbSNP: rs10510607
rs10510607
5 0.827 0.120 3 28244770 intron variant C/T snv 0.15 0.700 1.000 1 2016 2016
dbSNP: rs10743181
rs10743181
5 0.827 0.120 11 2208529 regulatory region variant A/G snv 0.77 0.700 1.000 1 2016 2016
dbSNP: rs10748781
rs10748781
11 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 0.700 1.000 1 2016 2016
dbSNP: rs10750899
rs10750899
5 0.827 0.120 11 58517478 intergenic variant G/A snv 0.95 0.700 1.000 1 2016 2016
dbSNP: rs10758669
rs10758669
6 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10761648
rs10761648
5 0.827 0.120 10 62594503 intron variant C/T snv 0.20 0.700 1.000 1 2016 2016
dbSNP: rs10775412
rs10775412
5 0.827 0.120 17 27542007 intron variant A/C snv 0.30 0.700 1.000 1 2016 2016