Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs375752214 0.708 0.400 7 150998541 missense variant C/T snv 4.1E-06 4.2E-05 22
rs1800553 0.742 0.240 1 94008251 missense variant C/T snv 4.7E-03 3.0E-03 17
rs61751374 0.776 0.160 1 94043413 missense variant G/A snv 1.7E-03 1.7E-03 10
rs6688832 0.752 0.440 1 9263851 missense variant G/A;C snv 0.28; 1.2E-04 10
rs76216585 0.807 0.160 12 89492071 stop gained C/A;G;T snv 8.5E-06; 2.7E-04 9
rs61750200 0.790 0.080 1 94098928 missense variant G/A;T snv 1.1E-04; 8.0E-06 8
rs768435443 0.807 0.080 1 94055128 missense variant A/G snv 4.0E-06 8
rs104894673
CRX
0.776 0.160 19 47839335 missense variant C/T snv 2.1E-05 8
rs104893968 0.790 0.200 6 42173762 missense variant C/G;T snv 4.0E-06; 1.2E-03 8
rs61750172 0.807 0.080 17 8014700 missense variant C/A;T snv 4.0E-06 8
rs61751392 0.827 0.080 1 94063250 missense variant A/G snv 1.5E-04 1.7E-04 7
rs121434631 0.807 0.080 6 42179248 missense variant C/G;T snv 4.0E-06 6
rs61750173 0.827 0.080 17 8014701 missense variant G/A snv 6
rs12086634 0.827 0.280 1 209706914 intron variant T/G snv 0.21 0.20 6
rs281865404 0.851 0.080 1 94014675 missense variant GG/CA mnv 4
rs61753033 0.882 0.080 1 94008767 missense variant A/G snv 2.0E-05 4
rs104894671
CRX
0.851 0.080 19 47836381 missense variant A/C snv 4
rs61748436
CRX
0.851 0.080 19 47836264 missense variant G/A snv 1.4E-05 4
rs28933695 0.851 0.080 17 8014699 missense variant G/C snv 4
rs61755815 0.851 0.080 6 42704463 missense variant T/G snv 4
rs62645926 0.851 0.080 6 42721784 missense variant T/G snv 4