Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10818684 1.000 0.040 9 122407651 intron variant C/T snv 0.62 2
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs10885390 0.925 0.080 10 112881038 regulatory region variant T/A snv 0.30 3
rs10887800
LOC101929727 ; RNLS
0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs10911021
LOC105371642 ; LINC01344
0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs10941191 1.000 0.040 5 34504693 intergenic variant C/A;T snv 3
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40 7
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 15
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs11071657 1.000 0.040 15 62141763 regulatory region variant A/G snv 0.31 3
rs11124945
PLEKHH2
1.000 0.040 2 43650017 intron variant A/G snv 0.21 3
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13 18
rs11196205
TCF7L2
0.827 0.200 10 113047288 intron variant G/A;C;T snv 7
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 9
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs11212617
C11orf65
0.827 0.200 11 108412434 intron variant C/A snv 0.49 7
rs1129844
CCL11
0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05 13
rs1131498
C1orf112 ; SELL
0.732 0.360 1 169707345 missense variant A/G snv 0.21 0.22 13
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs113296370
PLEKHH2
1.000 0.040 2 43636315 upstream gene variant A/C snv 0.17 3
rs1137933
NOS2
0.882 0.160 17 27778906 synonymous variant G/A snv 0.20 0.21 4
rs114202595
PAX4
0.882 0.120 7 127614533 missense variant G/A;T snv 1.2E-04; 9.1E-06 4
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs11547328
CDK4
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 27