Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs352140 0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs3804099 0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs3804100 0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs121917864 0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs5743836 0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs1800450 0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 26
rs1041981 0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
rs5743618 0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 25
rs3135932 0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11 23
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
rs8177374 0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs8193036 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs1718119 0.689 0.520 12 121177300 missense variant G/A;T snv 0.35; 4.0E-06 21
rs5743810 0.689 0.360 4 38828729 missense variant A/G snv 0.73 0.72 21
rs12212067 0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs2069705 0.695 0.440 12 68161231 intron variant G/A;C snv 19
rs2069837 0.724 0.520 7 22728408 intron variant A/C;G snv 18
rs352139 0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs2229094 0.776 0.320 6 31572779 missense variant T/C snv 0.27 0.27 17
rs7096206 0.708 0.480 10 52771925 upstream gene variant G/A;C;T snv 17
rs4804803 0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15