Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11249206
RUNX3 ; LOC105376878
0.851 0.160 1 24951491 intron variant C/T snv 0.48 4
rs9619311
TIMP3 ; SYN3
0.851 0.160 22 32800707 intron variant T/C snv 0.40 4
rs10775480
LOC105372093 ; SLC14A1
0.882 0.120 18 45737317 intron variant T/C snv 0.61 3
rs11077654
SLC39A11
0.882 0.120 17 73010373 intron variant A/C snv 0.69 3
rs11191438
AS3MT ; BORCS7-ASMT
0.882 0.120 10 102878107 intron variant G/A;C snv 3
rs11871756
SLC39A11
0.882 0.120 17 72730105 intron variant C/G snv 0.11 3
rs2042329
CWC27
0.882 0.120 5 64771925 intron variant T/C;G snv 3
rs3213255
XRCC1
0.882 0.120 19 43573355 intron variant G/A snv 0.60 3
rs3213356
XRCC1
0.882 0.120 19 43554087 intron variant C/T snv 0.60 3
rs3219493
MUTYH
0.882 0.120 1 45330597 intron variant G/C snv 0.92 0.93 3
rs4969054
SLC39A11
0.882 0.120 17 73016334 intron variant G/C snv 0.73 3
rs7832529
SLC20A2
0.882 0.120 8 42449295 intron variant T/C snv 0.24 3
rs8041357
ARID3B
0.882 0.120 15 74577097 intron variant T/C snv 6.6E-02 3
rs9624880
GRK3
0.882 0.120 22 25588025 intron variant C/T snv 3
rs9913017
SLC39A11
0.882 0.120 17 73014881 intron variant A/C;T snv 3
rs10811474 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 11
rs398652 0.752 0.240 14 56058851 intergenic variant G/A snv 0.24 10
rs1109324 0.827 0.160 6 43762018 intergenic variant G/T snv 0.15 5
rs833052 0.827 0.160 6 43755598 intergenic variant A/C snv 0.88 5
rs2764736 0.851 0.160 9 25067733 intergenic variant T/C snv 2.4E-02 4
rs710521 0.851 0.200 3 189928144 intergenic variant T/C snv 0.24 4
rs6464268 0.882 0.120 7 152684065 intergenic variant A/G snv 0.23 3
rs715021 0.882 0.120 2 221196620 intergenic variant C/G snv 0.26 3
rs1495741 0.827 0.240 8 18415371 regulatory region variant G/A snv 0.71 9
rs1547651 0.851 0.200 6 43762907 regulatory region variant A/T snv 0.15 4