Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10118757 0.827 0.120 9 21853340 intron variant A/G snv 0.26 7
rs1044925 0.827 0.120 1 179354603 3 prime UTR variant C/A;G snv 6
rs1063537 0.807 0.320 3 186856286 3 prime UTR variant C/T snv 9.6E-02 6
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10754558 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10937273 0.882 0.160 3 186831906 downstream gene variant G/A snv 0.33 4
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs1122608 0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs11536889 0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs12495941 0.851 0.280 3 186850391 intron variant G/T snv 0.35 5
rs1333040 0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs1333042 0.827 0.120 9 22103814 intron variant A/G snv 0.63 7
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs16147 0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs1648707 0.925 0.080 3 186833922 intergenic variant A/C snv 0.43 3
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 8
rs17114036 0.851 0.120 1 56497149 intron variant A/G snv 0.11 5
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs17366568 0.851 0.200 3 186852664 non coding transcript exon variant G/A snv 8.8E-02 6
rs174546 0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 17
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33