Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10208273 0.882 0.040 2 6383862 intergenic variant A/G snv 0.30 3
rs17111750 0.882 0.040 14 20442249 downstream gene variant C/T snv 0.30 3
rs231755 0.882 0.040 2 203888846 regulatory region variant G/C snv 0.11 3
rs7591996 0.882 0.040 2 6321289 intron variant A/C snv 0.57 3
rs8103992 0.882 0.040 19 19554834 regulatory region variant A/C;T snv 3
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs4148416
ABCC3
0.882 0.040 17 50676062 synonymous variant C/T snv 8.7E-02 0.10 3
rs1223868338
ACTA2 ; FAS
0.882 0.040 10 88990884 missense variant G/C snv 7.0E-06 3
rs1872328
ACYP2
0.827 0.120 2 54168122 intron variant G/A snv 7.3E-02 6
rs2086452
ADAMTS17
1.000 0.040 15 100188458 intron variant G/A;C snv 1
rs17206779
ADAMTS6
0.882 0.040 5 65151950 splice region variant C/G;T snv 0.48 3
rs1800544
ADRA2A
0.790 0.160 10 111076745 upstream gene variant G/C snv 0.59 12
rs553668
ADRA2A
0.807 0.160 10 111079821 3 prime UTR variant A/G;T snv 8
rs1215600806
ALPL
0.851 0.120 1 21564100 missense variant T/C snv 1.2E-05 4
rs1416572796
ALPL
0.851 0.120 1 21568170 missense variant G/T snv 4.0E-06 4
rs143358506
ALPL
0.851 0.120 1 21560674 missense variant T/C snv 8.0E-06 7.0E-06 4
rs1052667
ARHGAP35
0.882 0.040 19 47004177 3 prime UTR variant C/G;T snv 6
rs2372536
ATIC
0.827 0.160 2 215325297 missense variant C/G snv 0.33 0.25 5
rs122445099
ATRX
0.827 0.400 X 77520832 stop gained G/A snv 6
rs3787547
BCAS1
0.882 0.040 20 54067899 intron variant G/A snv 0.36 3
rs17655
BIVM-ERCC5 ; ERCC5
0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs2296147
BIVM-ERCC5 ; ERCC5
0.695 0.280 13 102846025 5 prime UTR variant T/C snv 0.38 21
rs235768
BMP2
0.807 0.160 20 6778468 missense variant A/G;T snv 0.67 8
rs1005464
BMP2
0.882 0.040 20 6775501 intron variant G/A snv 0.19 5
rs3178250
BMP2
0.827 0.080 20 6779554 3 prime UTR variant T/C snv 0.21 5