Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10165970 0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs10519097 0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11943456 0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs17024869 0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2585428 0.763 0.200 20 54170358 intron variant C/T snv 0.46 11
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4759314 0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs7581886 0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs895520 0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800440 0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 29
rs1045485 0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115