Source: GWASDB

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 9
rs925489
PTCSC2
0.882 0.080 9 97784318 intron variant C/T snv 0.71 5
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 4
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 4
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 3
rs10759944
PTCSC2
0.925 0.080 9 97794690 intron variant A/G snv 0.72 3
rs1443438
PTCSC2
0.827 0.080 9 97787746 intron variant T/A;C snv 3
rs7850258
PTCSC2
0.827 0.200 9 97786731 intron variant A/G snv 0.72 3
rs10984103 0.925 0.080 9 97876993 TF binding site variant A/C snv 0.68 2
rs7866436 0.925 0.080 9 97887814 intergenic variant G/A snv 0.70 2
rs907580 0.851 0.080 9 97860315 downstream gene variant T/A;C;G snv 2
rs925487 0.925 0.080 9 97874116 regulatory region variant C/A;T snv 2
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 2
rs2060793
CYP2R1
0.776 0.240 11 14893764 upstream gene variant A/G snv 0.63 2
rs10983700
PTCSC2
1.000 0.080 9 97775173 intron variant T/A;C snv 2
rs1588635
PTCSC2
1.000 0.080 9 97775520 intron variant A/C snv 0.72 2
rs7024345
PTCSC2
0.925 0.080 9 97832956 intron variant A/G snv 0.82 2
rs7030280
PTCSC2
1.000 0.080 9 97772985 intron variant C/T snv 0.72 2
rs7848973
PTCSC2
0.925 0.080 9 97826557 intron variant A/G snv 0.67 2
rs116909374 0.776 0.120 14 36269155 regulatory region variant C/T snv 2.3E-02 1
rs9344
CCND1
0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 1
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 1
rs6759952
DIRC3
1.000 0.080 2 217406996 intron variant T/A;C snv 1
rs966423
DIRC3
0.776 0.200 2 217445617 intron variant C/G;T snv 1
rs1443434
FOXE1
0.851 0.080 9 97855197 3 prime UTR variant G/T snv 0.63 1