Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 12
rs10510452 1.000 0.120 3 16583541 downstream gene variant A/G snv 0.22 2
rs4624820 0.851 0.240 5 142302223 regulatory region variant G/A snv 0.55 2
rs4635969 0.827 0.160 5 1308437 downstream gene variant G/A;T snv 2
rs7532231 1.000 0.120 1 104193445 intron variant A/G;T snv 0.39 2
rs8046148 1.000 0.120 16 50109033 intron variant A/G;T snv 2
rs2900333
ATF7IP
0.882 0.200 12 14500933 3 prime UTR variant C/A;G;T snv 2
rs2720460
CENPE
1.000 0.120 4 103133529 intron variant A/G snv 0.35 2
rs7040024
DMRT1
0.925 0.120 9 845516 intron variant A/C;G snv 2
rs755383
DMRT1
0.807 0.120 9 863635 intron variant C/T snv 0.54 2
rs210138
GGNBP1 ; BAK1
0.851 0.240 6 33574761 intron variant A/G snv 0.19 2
rs17021463
HPGDS
1.000 0.120 4 94303661 intron variant T/G snv 0.57 2
rs3782181
KITLG
0.882 0.120 12 88559784 intron variant C/A snv 0.65 2
rs12699477
MAD1L1
1.000 0.120 7 1929317 intron variant T/C snv 0.28 2
rs2839186
MCM3AP
1.000 0.120 21 46270154 intron variant C/T snv 0.42 2
rs6671895
MIR3659 ; MIR3659HG
1.000 0.120 1 38089354 intron variant C/A;T snv 4.9E-02 2
rs7010162
PRDM14
1.000 0.120 8 70064270 intron variant C/T snv 0.52 2
rs4888262
RFWD3
1.000 0.120 16 74636560 synonymous variant C/T snv 0.54 0.59 2
rs9905704
SEPTIN4-AS1
1.000 0.120 17 58555182 intron variant G/T snv 0.77 2
rs2072499
SLC25A44
1.000 0.120 1 156199819 non coding transcript exon variant A/G snv 0.34 0.43 2
rs3790672
UCK2
1.000 0.120 1 165904155 non coding transcript exon variant T/C snv 0.24 2
rs1508595 0.851 0.240 12 88592239 intron variant G/A;T snv 1
rs4699052 0.925 0.200 4 103216633 intergenic variant C/T snv 0.44 1
rs4474514
KITLG
0.827 0.240 12 88560182 intron variant G/A snv 0.65 1
rs995030
KITLG
0.776 0.320 12 88496894 3 prime UTR variant A/G snv 0.67 1