Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3025053 0.925 0.120 6 43785588 3 prime UTR variant G/A snv 8.6E-02 2
rs10434 0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs3025040 0.882 0.120 6 43785314 3 prime UTR variant C/T snv 0.15 3
rs1479430148 1.000 0.120 6 43784861 3 prime UTR variant A/T snv 1
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs771561387 1.000 0.080 6 43784557 missense variant C/G;T snv 4.0E-06; 1.2E-05 2
rs748984440 1.000 0.040 6 43784546 stop lost A/C snv 4.0E-06 2
rs3025036 1.000 0.080 6 43783932 non coding transcript exon variant G/A;C;T snv 1
rs3025035 0.851 0.240 6 43783622 non coding transcript exon variant C/T snv 0.14 4
rs3025033 0.807 0.360 6 43783338 non coding transcript exon variant A/G snv 0.18 6
rs3025030 0.882 0.200 6 43782850 non coding transcript exon variant G/C snv 0.13 3
rs140461341 6 43782078 missense variant G/A snv 3.6E-05 4.2E-05 2
rs752907384 0.827 0.200 6 43782077 missense variant C/G;T snv 8.0E-06 6
rs749491856 1.000 6 43782071 missense variant A/C snv 1
rs1229919945 1.000 0.040 6 43782041 missense variant T/C snv 1
rs1287276985 0.790 0.200 6 43782020 missense variant T/A;C snv 4.0E-06; 4.0E-06 7.0E-06 7
rs376388064 6 43782006 missense variant C/T snv 2.8E-05 3.5E-05 1
rs1188254133 0.851 0.240 6 43781990 missense variant T/G snv 7.0E-06 4
rs3025021 0.882 0.160 6 43781426 non coding transcript exon variant T/C snv 0.70 4
rs3025020 0.882 0.240 6 43781373 non coding transcript exon variant C/T snv 0.24 3
rs752153816 0.882 0.120 6 43780848 missense variant G/A;C snv 4.0E-06; 4.0E-06; 1.2E-05; 3.6E-05 3
rs777846438 0.925 0.240 6 43780801 splice region variant C/T snv 4.4E-05 6.3E-05 2
rs141138308 1.000 0.040 6 43780784 missense variant C/A;T snv 4.0E-06; 2.8E-05 1
rs774265827 6 43780773 missense variant G/A;T snv 8.0E-06; 2.0E-05 1
rs138551969 1.000 0.040 6 43780749 missense variant A/G snv 1.2E-05 3.5E-05 4