Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs10012 0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 16
rs1004072779
ERG
0.925 0.080 21 38403547 missense variant T/C snv 2.1E-05 2
rs10046 0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43 18
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs10090154 0.807 0.160 8 127519892 intergenic variant T/A;C snv 7
rs1012477 0.827 0.160 1 7798075 intron variant G/C snv 0.16 8
rs1016343 0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20 8
rs10165970 0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs10175368 0.925 0.080 2 38080719 intron variant C/T snv 0.23 4
rs10187424 0.925 0.080 2 85567174 intron variant T/A;C snv 2
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 7
rs1034528 0.882 0.120 1 11189075 intron variant G/C snv 0.30 5
rs1034866440
AR
0.851 0.160 X 67643401 missense variant G/A snv 5.7E-06 4
rs1041258260 0.925 0.080 19 43552170 missense variant C/T snv 8.0E-06 1.4E-05 2
rs1042489 0.851 0.160 17 78224125 3 prime UTR variant T/C snv 0.40 5
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042636 0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 23
rs10426628 0.925 0.080 19 48589173 intron variant A/G snv 0.78 2
rs10432782 0.807 0.160 21 31664078 intron variant T/G snv 0.19 7
rs1045485 0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs1045531 0.882 0.080 8 142682129 synonymous variant C/A snv 0.45 0.44 3
rs10459592 0.925 0.080 15 51243944 intron variant T/G snv 0.49 2
rs1046040 0.925 0.080 19 1095515 upstream gene variant G/A snv 0.21 2