Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2352028 0.851 0.080 13 91792975 intron variant C/G;T snv 6
rs2564978 0.827 0.080 1 207321071 upstream gene variant T/C snv 0.77 6
rs2835267 0.827 0.080 21 36074727 intron variant T/C snv 0.63 6
rs4513061 0.807 0.080 15 86428401 intron variant G/A;T snv 6
rs503464 0.851 0.080 15 78565554 5 prime UTR variant T/A snv 0.28 6
rs7177514 0.882 0.080 15 78615064 intron variant C/G;T snv 6
rs767935771
AXL
0.827 0.080 19 41259690 missense variant T/C snv 1.6E-05 5.6E-05 6
rs772399455 0.851 0.080 2 15942096 missense variant G/A;C snv 4.0E-06 6
rs78768932
PXN
0.882 0.080 12 120222977 missense variant C/G;T snv 5.4E-03 5.4E-03 6
rs7937 0.851 0.080 19 40796801 3 prime UTR variant C/A;T snv 0.49 6
rs8042059 0.882 0.080 15 78615517 intron variant A/C;T snv 6
rs9895829 0.807 0.080 17 7675361 5 prime UTR variant A/G snv 7.4E-02 6
rs1019340046 0.882 0.080 17 7674225 missense variant C/T snv 5
rs10254120 0.851 0.080 7 6005996 missense variant C/A;G;T snv 7.2E-02 5
rs1026411 0.827 0.080 8 127014165 intron variant G/A;C snv 0.25 5
rs121917737 0.827 0.080 10 79557264 missense variant C/A snv 5
rs121917738 0.827 0.080 10 79557363 missense variant A/G snv 5
rs12587742 0.851 0.080 14 72926683 intron variant G/A snv 0.18 5
rs1275824108 0.851 0.080 14 54399922 missense variant A/G snv 7.0E-06 5
rs1329032366 0.882 0.080 4 94654530 missense variant A/G snv 4.0E-06 5
rs1330189219 0.882 0.080 6 31573570 synonymous variant C/T snv 4.0E-06 5
rs1423493595 0.851 0.080 20 50082836 missense variant G/A snv 4.0E-06 7.0E-06 5
rs1454694 0.827 0.080 4 181276794 intergenic variant T/C snv 0.20 5
rs1487151044 0.851 0.080 10 31510817 missense variant T/C snv 5
rs3124599 0.851 0.080 9 136509318 intron variant G/A snv 0.13 5