Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10849915
CCDC63
0.925 0.080 12 110895818 intron variant T/C snv 0.39 3
rs10897164
LRRC10B
11 61510303 3 prime UTR variant A/G snv 0.13 3
rs1090107
NEIL2
8 11775019 intron variant A/G;T snv 2
rs10935068 3 133543963 upstream gene variant T/A;G snv 1
rs10935070
TOPBP1
3 133623144 missense variant T/C;G snv 0.29; 4.0E-06 1
rs10935073
INHCAP ; TF
3 133720340 intron variant T/C snv 0.34 1
rs10953881 7 118968071 intergenic variant C/G;T snv 1
rs10953885 7 118968349 intergenic variant T/A;C snv 1
rs10955992 8 120860224 intergenic variant A/C;T snv 2
rs10957054
UBXN2B
8 58423997 intron variant C/T snv 0.73 3
rs11023906
SOX6
11 16302860 intron variant G/A snv 0.17 3
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs11066015
ACAD10
0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03 5
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs11072518 15 74942269 upstream gene variant T/A;C snv 3
rs1107413
SRPRB ; LOC105374116
3 133805873 missense variant G/C snv 0.22 0.20 1
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs11102001
GSTM5 ; EPS8L3
0.925 0.080 1 109757069 missense variant G/A snv 9.4E-02 0.16 4
rs11105352
ATP2B1
12 89632685 intron variant G/A snv 0.14 4
rs1111336 2 28435029 regulatory region variant A/C;G snv 2
rs11128951 3 20334054 intron variant A/G snv 0.19 1
rs111478946
ATP2B1
12 89665065 intron variant G/A snv 0.14 4
rs11154376
LOC105377991
6 126879498 intron variant A/G snv 0.36 2
rs11208264
PGM1
1 63659401 intron variant T/C snv 0.30 1
rs112259268 17 43797377 downstream gene variant C/A snv 1.9E-02 6