Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 7
rs10983755 0.790 0.320 9 117702392 upstream gene variant G/A snv 3.2E-02 7
rs2735839 0.827 0.160 19 50861367 upstream gene variant A/C;G snv 7
rs17144046 0.882 0.120 10 8564051 intergenic variant A/G snv 0.28 4
rs11084596 1.000 0.040 19 31614073 regulatory region variant T/C snv 0.35 3
rs11199879 1.000 0.040 10 121285698 regulatory region variant T/C snv 0.18 3
rs2555019 1.000 0.040 12 114230813 intergenic variant T/C;G snv 3
rs148678804 1.000 0.040 10 22138360 intergenic variant G/A;T snv 2
rs200476 1.000 0.040 6 27800570 intergenic variant A/T snv 0.28 2
rs7906649 1.000 0.040 10 22021369 intergenic variant G/A snv 0.60 2
rs10786938 1.000 0.040 10 106280012 intergenic variant G/C;T snv 1
rs141179786 1.000 0.040 18 53662174 intergenic variant A/G;T snv 2.2E-02 1
rs16902947 1.000 0.040 5 36308995 intergenic variant A/G snv 0.22 1
rs6078585 1.000 0.040 20 12447612 intergenic variant C/A;T snv 1
rs137852569
AR
0.752 0.320 X 67686030 missense variant G/A snv 9.4E-06 10
rs6152
AR
0.763 0.240 X 67545785 synonymous variant G/A snv 0.15 0.28 9
rs1034866440
AR
0.851 0.160 X 67643401 missense variant G/A snv 5.7E-06 4
rs3803185
ARL11
0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 19
rs2556378
BCL11A
1.000 0.040 2 60535367 3 prime UTR variant T/G snv 0.81 3
rs72878024
BET1L ; ODF3
1.000 0.040 11 199492 missense variant G/A snv 6.4E-02 6.4E-02 2
rs10035432
C5orf46
1.000 0.040 5 147855193 upstream gene variant G/A snv 0.18 1
rs677394
C5orf66
1.000 0.040 5 135271869 intron variant G/C;T snv 2
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68