Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 4
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 3
rs3803662
CASC16
0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 3
rs3814113 0.827 0.200 9 16915023 upstream gene variant T/C snv 0.41 3
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 3
rs11651755
HNF1B
0.763 0.160 17 37739849 intron variant T/C snv 0.52 2
rs13281615
CASC8 ; POU5F1B ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43 2
rs17251221
CASR
0.724 0.360 3 122274400 intron variant A/G snv 0.11 2
rs2153271
BNC2
0.925 0.160 9 16864523 intron variant C/T snv 0.43 2
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 2
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58 2
rs367899983
BNC2
1.000 0.120 9 16864524 intron variant GTCT/- delins 4.2E-05 2
rs10088218
LINC00824
0.851 0.120 8 128531703 intron variant G/A snv 0.13 1
rs10756819
BNC2
1.000 0.120 9 16858086 intron variant G/A;C;T snv 1
rs10810666 1.000 0.120 9 16911668 intergenic variant C/T snv 0.14 1
rs10962656 1.000 0.120 9 16877790 intergenic variant G/A snv 0.10 1
rs11782652
CHMP4C
0.851 0.120 8 81741409 intron variant A/G snv 6.6E-02 1
rs12373237
LAMA3
0.851 0.200 18 23845972 intron variant G/A snv 0.47 1
rs12379183
BNC2
1.000 0.120 9 16865701 intron variant A/G snv 0.26 1
rs12379687
BNC2
1.000 0.120 9 16854369 intron variant G/A;T snv 1
rs1243180
MLLT10
0.790 0.160 10 21626690 intron variant T/A snv 0.23 1
rs12451939
MED13
1.000 0.120 17 61970281 intron variant A/G snv 2.6E-02 1
rs1256030
ESR2
0.827 0.240 14 64280452 intron variant A/G;T snv 1
rs1256031
ESR2
0.790 0.200 14 64279461 intron variant G/A;T snv 0.57 1
rs12937080
BRIP1
1.000 0.120 17 61852376 intron variant A/G;T snv 1