Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10094574 8 77203831 intergenic variant G/A;T snv 1
rs10150590 14 40456677 intergenic variant A/C snv 0.63 1
rs10170108 2 136692386 intergenic variant G/A snv 0.53 1
rs10226266 7 32901507 intergenic variant A/G snv 0.63 1
rs1038903 4 28750432 intergenic variant C/T snv 0.79 1
rs10740399 10 72300443 intergenic variant A/G snv 0.53 1
rs10786610 10 100880906 TF binding site variant G/C;T snv 1
rs10820310 9 102923803 downstream gene variant A/G snv 0.28 1
rs10860153 12 97147754 intron variant A/G snv 0.36 1
rs10874340 1 82793397 intron variant G/A;T snv 1
rs10908948 9 89806050 intron variant G/A snv 0.41 1
rs10940138 5 67898641 intron variant C/T snv 0.21 1
rs10941225 5 34961375 downstream gene variant T/A snv 0.32 1
rs10960303 9 11839805 intron variant C/A snv 0.19 1
rs10980854 9 111288077 upstream gene variant G/A snv 0.12 1
rs10980921 9 111517632 intergenic variant T/C snv 0.15 1
rs10984237 9 118806262 intergenic variant T/C;G snv 1
rs112335739 12 47450879 intergenic variant C/T snv 8.0E-02 1
rs112753638 2 202334496 upstream gene variant C/A;T snv 1
rs114489117 5 93612779 downstream gene variant T/A snv 6.4E-02 1
rs115260227 4 103853541 intergenic variant A/G snv 5.4E-03 1
rs11534296 9 80667487 intergenic variant G/A;C snv 1
rs11578152 1 102111465 intergenic variant A/G;T snv 1
rs11703376 22 49282787 intergenic variant C/T snv 0.20 1
rs12148769 15 23906947 intergenic variant G/A snv 8.9E-02 1