Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs121434569
EGFR-AS1 ; EGFR
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs2043211
CARD8
0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs28933385
PRNP
0.695 0.320 20 4699818 missense variant G/A snv 4.0E-06 25
rs2814778
CADM3-AS1 ; ACKR1
0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 24
rs2383206
CDKN2B-AS1
0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs72653744
ABCC6
0.807 0.320 16 16163009 stop gained G/A snv 1.7E-04 1.2E-04 14
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 13
rs5068
NPPA ; NPPA-AS1 ; CLCN6
0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13
rs12041331
PEAR1
0.776 0.200 1 156899922 intron variant G/A snv 0.19 11
rs10846744
SCARB1
0.763 0.160 12 124827879 intron variant G/C snv 0.32 11
rs2297595
DPYD
0.776 0.320 1 97699535 missense variant T/C snv 8.5E-02 8.1E-02 10
rs120074192
KCNQ1
0.763 0.120 11 2527959 missense variant A/G snv 10
rs4242382 0.763 0.240 8 127505328 intergenic variant A/G;T snv 9
rs11571836
BRCA2
0.827 0.200 13 32399302 3 prime UTR variant A/G;T snv 6
rs1801160
DPYD ; DPYD-AS1
0.807 0.240 1 97305364 missense variant C/T snv 4.7E-02 3.9E-02 6
rs1799943
BRCA2
0.925 0.080 13 32316435 5 prime UTR variant G/A;C;T snv 0.25 5
rs1049550
ANXA11
0.882 0.160 10 80166946 missense variant G/A;C snv 0.42; 4.2E-06 4