Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12718945 1.000 0.040 7 55125270 intron variant T/G snv 0.51 1
rs3752651 1.000 0.040 7 55161850 intron variant T/C snv 0.15 1
rs845552 1.000 0.040 7 55177814 intron variant A/G snv 0.43 1
rs17749 1.000 0.040 6 38676020 3 prime UTR variant C/T snv 1
rs1345354331 1.000 0.040 3 49358221 missense variant A/C;T snv 6.8E-06; 6.8E-06 1
rs643788 1.000 0.040 11 119097048 missense variant T/C snv 0.42 0.38 1
rs3093739 1.000 0.040 13 108215053 intron variant A/G snv 8.8E-02 1
rs749124997 1.000 0.040 12 102402539 missense variant C/T snv 4.0E-06 1
rs770617145 1.000 0.040 17 49512716 missense variant G/A snv 3.4E-05 1
rs573905 1.000 0.040 11 118701558 intron variant A/G snv 0.56 1
rs10764901 1.000 0.040 10 129716598 intron variant A/G snv 0.62 1
rs4598633 1.000 0.040 11 96278187 intron variant T/A;C snv 1
rs485842 1.000 0.040 11 96290050 intron variant C/T snv 0.26 1
rs7938889 1.000 0.040 11 96231355 intron variant C/T snv 0.48 1
rs1339499 1.000 0.040 9 125644174 intron variant T/C snv 0.29 1
rs473426 1.000 0.040 9 125644709 intron variant G/C snv 0.44 1
rs1982266 1.000 0.040 10 52770876 intron variant A/G;T snv 1
rs17138945
MET
1.000 0.040 7 116703812 intron variant T/G snv 7.3E-02 1
rs7727115 1.000 0.040 5 160474732 intron variant G/T snv 0.17 1
rs2961920 1.000 0.040 5 160484499 intron variant C/A snv 0.70 1
rs11730
NMI
1.000 0.040 2 151270497 3 prime UTR variant A/G snv 0.36 1
rs2194492
NMI
1.000 0.040 2 151289680 5 prime UTR variant G/C snv 0.53 1
rs3854012
NMI
1.000 0.040 2 151280592 intron variant C/T snv 0.44 1
rs6734376
NMI
1.000 0.040 2 151288153 intron variant T/C snv 0.27 1
rs372951639 1.000 0.040 16 69718484 missense variant A/T snv 1.6E-05 3.5E-05 1