Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 12
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 10
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 9
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 9
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 9
rs1327235 20 10988382 intron variant A/G snv 0.46 7
rs6015450
ZNF831
20 59176062 intron variant A/G snv 0.14 7
rs805303
BAG6
0.925 0.160 6 31648589 intron variant G/A snv 0.45 7
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs381815
PLEKHA7
1.000 0.040 11 16880721 intron variant C/A;T snv 0.24 6
rs419076
MECOM
3 169383098 intron variant T/A;C snv 6
rs932764
PLCE1
10 94136183 intron variant A/G snv 0.38 6
rs11636952
LMAN1L
15 74821981 intron variant T/C snv 0.48 5
rs12940887
ZNF652
17 49325445 intron variant C/T snv 0.28 5
rs12946454
ACBD4 ; PLCD3
0.925 0.040 17 45130754 intron variant A/T snv 0.21 5
rs1573643
FURIN
15 90877743 intron variant T/C snv 0.33 5
rs1731249
KCNK3
2 26697157 intron variant T/A snv 0.48 5