Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7212142
RPTOR
0.827 0.200 17 80650141 intron variant G/A snv 0.50 5
rs887569
EZH2
0.882 0.120 7 148808210 intron variant C/T snv 0.73 5
rs10094872
CASC11
0.882 0.200 8 127707639 intron variant A/T snv 0.33 4
rs10743980
LRP6
0.882 0.120 12 12259861 intron variant T/A;C;G snv 4
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
rs17650301
POLG2 ; MILR1
0.925 0.120 17 64483156 intron variant A/C snv 0.23 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
rs62185668 0.925 0.120 20 10981287 intron variant C/A snv 0.19 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
rs2836007
KCNJ6
0.925 0.120 21 37834589 intron variant C/T snv 0.21 2
rs4510656
CDKAL1
0.925 0.120 6 20766466 intron variant C/A snv 0.39 2
rs5003154
PAG1
0.925 0.120 8 81074718 intron variant T/C;G snv 2
rs6104690
LINC02871
0.925 0.120 20 11007451 intron variant G/A;T snv 2