Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1051266 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs3804100 0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs4149584 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 24
rs35829419 0.689 0.560 1 247425556 missense variant C/A snv 3.9E-02 3.3E-02 23
rs2069705 0.695 0.440 12 68161231 intron variant G/A;C snv 19
rs28940580 0.742 0.560 16 3243447 missense variant C/A;G;T snv 1.0E-04; 8.0E-06 17
rs2146323 0.752 0.480 6 43777358 non coding transcript exon variant C/A snv 0.31 13
rs1064797245 0.776 0.280 19 41970540 missense variant G/A snv 12
rs2227956 0.752 0.400 6 31810495 missense variant G/A;C;T snv 0.87 12
rs3811047 0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60 10
rs28934897
MVK
0.790 0.400 12 109596515 missense variant G/A snv 1.6E-03 1.5E-03 10
rs137854601 0.776 0.120 3 38551022 stop gained C/A;T snv 4.0E-06 10
rs72554640 0.882 0.160 X 78011239 stop gained C/T snv 9
rs121918622 0.790 0.080 2 165992332 missense variant C/A;T snv 4.0E-06 9
rs1554785242 0.882 0.160 9 133426240 missense variant G/T snv 8
rs1554791280 0.882 0.160 9 133442718 missense variant T/C snv 8
rs2229291 0.827 0.200 1 53210729 missense variant T/G snv 2.3E-02 1.5E-02 8
rs61752115 0.807 0.320 2 61048535 missense variant T/C snv 4.0E-06 7
rs199473605 0.851 0.120 3 38560374 missense variant C/G;T snv 4.8E-05; 4.0E-06 7