Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 10
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 9
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 5
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 5
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 4
rs10804591 3 129615390 intergenic variant C/A snv 0.63 4
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 4
rs5015480 0.851 0.120 10 92705802 downstream gene variant C/T snv 0.42 4
rs10245353 7 25818994 intergenic variant C/A snv 0.16 3
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 3
rs7923837 0.882 0.160 10 92722160 intergenic variant G/A;T snv 3
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 2
rs12779790 0.882 0.120 10 12286011 intergenic variant A/G snv 0.17 2
rs2383208 0.882 0.120 9 22132077 downstream gene variant A/G;T snv 0.18 2
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 2
rs7936247 1.000 0.040 11 92956866 intergenic variant G/T snv 0.37 2
rs10229583 1.000 0.080 7 127606849 downstream gene variant G/A snv 0.23 1
rs137852671
ABCC8
0.790 0.160 11 17394295 missense variant C/T snv 1
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 6
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 1
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 5
rs3789678
AGT
1.000 0.040 1 230713736 intron variant C/T snv 0.15 1
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 7
rs1552224
ARAP1
1.000 0.080 11 72722053 5 prime UTR variant A/C snv 0.12 3
rs2975760
CAPN10
1.000 0.080 2 240591746 non coding transcript exon variant T/C snv 0.12 2