Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10754558 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs12212067 0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs352139 0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs1861494 0.716 0.400 12 68157629 intron variant C/T snv 0.75 15
rs4804803 0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs3751143 0.742 0.480 12 121184501 missense variant A/C;G snv 0.19; 4.0E-06 12
rs5030737 0.752 0.360 10 52771482 missense variant G/A snv 5.6E-02 5.0E-02 11
rs10065172 0.790 0.200 5 150848436 synonymous variant C/T snv 0.17 0.21 8
rs754342091 0.790 0.200 9 117712421 missense variant A/G snv 3.2E-05 1.4E-05 7
rs1816702 0.827 0.120 4 153688371 non coding transcript exon variant T/C snv 0.79 6
rs2234711 0.827 0.080 6 137219383 5 prime UTR variant A/G snv 0.43 6
rs17525495 0.882 0.080 12 96035599 5 prime UTR variant G/A snv 9.9E-02 4
rs5743278 0.882 0.080 16 50712085 missense variant C/G snv 3.2E-03 1.3E-02 3
rs4958843 0.925 0.080 5 150845362 upstream gene variant T/C snv 0.21 2
rs72553867 0.925 0.080 5 150848404 missense variant C/A;T snv 4.9E-02 2