Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10036748 0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs1063320 0.752 0.360 6 29830972 3 prime UTR variant C/G;T snv 12
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs2069705 0.695 0.440 12 68161231 intron variant G/A;C snv 19
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2280964 0.882 0.200 X 71618204 intron variant C/A;G;T snv 3
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs3129890 0.827 0.280 6 32446496 downstream gene variant T/A;C snv 5
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs396991 0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs549908 0.752 0.440 11 112150193 synonymous variant T/A;G snv 4.2E-06; 0.29 10
rs555743307 0.695 0.440 16 27342243 missense variant G/A;T snv 3.6E-05; 2.9E-04 20
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 28
rs10917661 0.882 0.160 1 161671427 stop gained C/T snv 2.8E-05 3
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98