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: rs11205303
rs11205303
9 0.882 0.120 1 149934520 missense variant T/C snv 0.33 0.29 0.700 1.000 1 2015 2015
dbSNP: rs12534093
rs12534093
3 7 23463355 intron variant T/A snv 0.18 0.700 1.000 1 2015 2015
dbSNP: rs1380294
rs1380294
2 4 18022498 upstream gene variant C/T snv 0.25 0.700 1.000 1 2015 2015
dbSNP: rs143384
rs143384
17 0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 0.700 1.000 1 2015 2015
dbSNP: rs1567865
rs1567865
1 20 49265430 intron variant C/T snv 0.15 0.700 1.000 1 2015 2015
dbSNP: rs1812175
rs1812175
6 4 144653692 intron variant A/G snv 0.79 0.700 1.000 1 2015 2015
dbSNP: rs1984119
rs1984119
2 9 95606479 upstream gene variant T/C snv 0.24 0.700 1.000 1 2015 2015
dbSNP: rs2280470
rs2280470
3 15 88852395 intron variant A/G snv 0.68 0.700 1.000 1 2015 2015
dbSNP: rs592229
rs592229
2 1.000 0.080 6 31962664 intron variant G/A;C;T snv 4.0E-06; 4.5E-05; 0.61 0.700 1.000 1 2015 2015
dbSNP: rs6470764
rs6470764
3 8 129713419 intron variant C/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs724016
rs724016
5 1.000 0.040 3 141386728 5 prime UTR variant A/G snv 0.52 0.700 1.000 1 2015 2015
dbSNP: rs7536458
rs7536458
5 1 118321979 intergenic variant T/G snv 0.23 0.700 1.000 1 2015 2015
dbSNP: rs7970350
rs7970350
5 12 65966384 downstream gene variant C/T snv 0.48 0.700 1.000 1 2015 2015
dbSNP: rs9385399
rs9385399
1 6 126437887 intron variant G/T snv 0.42 0.700 1.000 1 2015 2015