Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs121912438 0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs75932628 0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs11558538 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 19
rs1475170339 0.732 0.240 16 1792325 missense variant T/C;G snv 18
rs7120118 0.716 0.360 11 47264739 intron variant T/C snv 0.38 18
rs5848 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs2695121 0.716 0.280 19 50377484 5 prime UTR variant T/C snv 0.70 16
rs80265967 0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03 16
rs121912443 0.732 0.160 21 31663857 missense variant A/G snv 15
rs367543041 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 15
rs74315431 0.732 0.080 20 58418318 missense variant C/T snv 4.0E-06 15
rs11868035 0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33 14
rs387906789
VCP
0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 14