Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3131837 0.882 0.080 1 100252204 non coding transcript exon variant C/G snv 0.80 3
rs7158663 0.827 0.240 14 100853087 non coding transcript exon variant A/G snv 0.42 9
rs4081134 0.790 0.160 14 100855451 non coding transcript exon variant G/A snv 0.29 7
rs1174612410 0.882 0.080 7 100860016 missense variant A/G snv 4.0E-06 7.0E-06 3
rs4919510 0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs12894467 0.807 0.080 14 101041390 non coding transcript exon variant C/T snv 0.51 0.50 6
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs6092 0.807 0.200 7 101128436 missense variant G/A snv 9.5E-02 8.0E-02 6
rs5030807
VHL
0.851 0.320 3 10142113 missense variant T/A;C snv 5
rs1446876735
VHL
1.000 0.080 3 10142164 missense variant G/A snv 1
rs3218977 0.807 0.240 2 102024739 3 prime UTR variant A/G snv 0.14 6
rs2072472 0.732 0.200 2 102026557 intron variant A/G snv 0.24 13
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs3774934 0.851 0.080 4 102506319 intron variant A/C;G;T snv 4
rs13117745 0.882 0.080 4 102557546 intron variant C/T snv 0.18 3
rs230541 0.882 0.080 4 102576628 intron variant G/A snv 0.58 3
rs1801 0.882 0.080 4 102579897 intron variant C/G;T snv 3
rs4648127 0.882 0.080 4 102614748 intron variant C/T snv 4.3E-02 3
rs35866072 0.716 0.360 11 102713373 missense variant T/G snv 6.0E-02 9.8E-02 17
rs34009635 0.716 0.360 11 102713445 missense variant A/G snv 2.5E-03 6.2E-04 17
rs1144393 0.851 0.160 11 102798678 intron variant T/C snv 0.30 5
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs678815 0.851 0.080 11 102843046 intron variant G/A;C snv 4
rs3025058 0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26