Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs656319 8 9956901 intergenic variant A/G snv 0.49 3
rs932764
PLCE1
10 94136183 intron variant A/G snv 0.38 6
rs9561252 13 93077032 intergenic variant A/G snv 7.2E-02 2
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs1573643
FURIN
15 90877743 intron variant T/C snv 0.33 5
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 12
rs2681485
ATP2B1
12 89631845 intron variant G/A;T snv 3
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs7823056 8 8525195 intergenic variant A/G snv 0.55 3
rs2980755 8 8506173 intergenic variant A/G snv 0.46 3
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 10
rs8010717
LOC107984630
14 79944098 intron variant T/C snv 0.29 4
rs16890334 6 78846449 intergenic variant T/C snv 1.9E-03 3
rs4573996 18 78734592 intergenic variant G/A snv 0.12 2
rs12899430
COX5A
15 74936759 intron variant T/C snv 0.37 2
rs1133322
COX5A
15 74920016 3 prime UTR variant A/G snv 0.38 2
rs11636952
LMAN1L
15 74821981 intron variant T/C snv 0.48 5
rs2301249
CSK
15 74800043 intron variant T/C snv 0.66 3
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs8078051
TTYH2
17 74255101 intron variant G/A snv 4.4E-02 2
rs8002688
PIBF1
13 72985844 intron variant C/T snv 0.12 2
rs2306363
SIPA1
11 65638129 5 prime UTR variant G/T snv 0.15 7
rs4590817
CABCOCO1
10 61707795 intron variant G/C snv 0.15 5