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: rs9614326
rs9614326
1 22 44103463 non coding transcript exon variant A/C snv 3.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs11655160
rs11655160
1 17 10989753 intergenic variant G/A snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs11179580
rs11179580
1 12 73192799 intron variant C/T snv 0.27 0.700 1.000 1 2014 2014
dbSNP: rs1606958
rs1606958
1 12 73266151 intergenic variant C/A snv 0.27 0.700 1.000 1 2014 2014
dbSNP: rs10161441
rs10161441
1 12 73136489 intron variant C/T snv 0.27 0.700 1.000 1 2014 2014
dbSNP: rs10879561
rs10879561
1 12 73139547 intron variant A/T snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs2176205
rs2176205
1 12 73159438 non coding transcript exon variant C/T snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs7302852
rs7302852
1 12 73163388 intron variant C/A snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs1976730
rs1976730
1 12 73159402 non coding transcript exon variant A/G snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs10879572
rs10879572
1 12 73157791 upstream gene variant C/T snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs10879569
rs10879569
1 12 73157101 upstream gene variant A/G snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs12811378
rs12811378
1 12 73160134 intron variant C/G snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs12826112
rs12826112
1 12 73162120 intron variant T/C snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs1516058
rs1516058
1 12 73137889 intron variant T/C snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs12813018
rs12813018
1 12 73160218 intron variant T/A snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs34144381
rs34144381
1 12 73153778 intergenic variant A/T snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs7311904
rs7311904
1 12 73154963 upstream gene variant C/T snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs10879568
rs10879568
1 12 73156497 upstream gene variant C/T snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs2853646
rs2853646
1 1 156219835 intron variant C/T snv 0.30 0.700 1.000 1 2014 2014
dbSNP: rs2540183
rs2540183
1 1 156195094 intron variant C/G snv 0.30 0.700 1.000 1 2014 2014
dbSNP: rs2758598
rs2758598
1 1 156224548 intron variant G/A snv 0.30 0.700 1.000 1 2014 2014
dbSNP: rs2758600
rs2758600
1 1 156225414 intron variant C/T snv 0.30 0.700 1.000 1 2014 2014
dbSNP: rs2244144
rs2244144
1 1 156214807 intron variant G/A snv 0.30 0.700 1.000 1 2014 2014
dbSNP: rs2853643
rs2853643
1 1 156215040 intron variant G/A snv 0.30 0.700 1.000 1 2014 2014
dbSNP: rs1060604
rs1060604
1 1 156214477 intron variant T/C snv 0.30 0.700 1.000 1 2014 2014