Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11237982 1.000 0.080 11 79730650 intergenic variant T/C snv 0.18 2
rs117905930 1.000 0.080 9 88973603 intron variant C/A;T snv 2
rs147906088 1.000 0.080 7 54496119 intergenic variant C/A;T snv 2
rs10058621 5 51259335 intergenic variant T/C snv 6.0E-02 1
rs11074779 16 26440122 intergenic variant T/C snv 0.16 1
rs12436690 14 97119552 intron variant G/A snv 0.12 1
rs12990252 2 35861457 intergenic variant G/C snv 0.18 1
rs13166268 5 121024223 intergenic variant C/G snv 9.2E-02 1
rs140454225 16 1003856 upstream gene variant T/C;G snv 1
rs1449587 13 48839332 regulatory region variant C/T snv 0.31 1
rs145471199 7 9407441 intergenic variant A/G;T snv 1
rs150900094 15 87284961 intergenic variant A/C snv 2.9E-02 1
rs35551159 12 60075450 intergenic variant C/A;T snv 1
rs4762194 12 97789941 intergenic variant G/A snv 0.20 1
rs4776997 15 67858585 intron variant A/G;T snv 0.77 1
rs6020113 20 37674643 upstream gene variant G/A snv 9.2E-02 1
rs6813517 4 167601600 intergenic variant T/C snv 0.17 1
rs74938950 20 12281822 intron variant C/T snv 1.2E-02 1
rs7557162 2 177057129 intron variant A/C;T snv 1
rs8073765 17 13726414 regulatory region variant T/C snv 0.26 1
rs932350 1 4793628 downstream gene variant T/A;C snv 1
rs9528384 13 61728432 regulatory region variant A/G snv 0.23 1
rs5747035
ADA2
22 17237716 intron variant T/C snv 0.15 1
rs6830160
ANAPC4
4 25377604 intron variant G/A;T snv 8.1E-02 1
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43