Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1926203
FAS ; STAMBPL1 ; ACTA2
0.882 0.160 10 88967577 intron variant C/A snv 0.59 2
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58 2
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 2
rs1859962
CASC17
0.882 0.160 17 71112612 intron variant G/T snv 0.56 2
rs3123078 0.882 0.160 10 46070851 regulatory region variant G/A snv 0.55 2
rs4624820 0.851 0.240 5 142302223 regulatory region variant G/A snv 0.55 3
rs12500426
PDLIM5
0.851 0.240 4 94593458 intron variant A/C snv 0.54 2
rs10993994
MSMB
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54 3
rs10896449 0.827 0.200 11 69227200 intergenic variant A/G snv 0.53 2
rs2981579
FGFR2
0.776 0.280 10 121577821 intron variant A/G snv 0.53 2
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 9
rs4430796
HNF1B
0.790 0.280 17 37738049 intron variant A/G snv 0.52 5
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 4
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 2
rs1512268
LOC107986930
0.851 0.160 8 23668950 intergenic variant T/C snv 0.50 2
rs6545977 0.882 0.160 2 63074029 regulatory region variant G/A snv 0.50 2
rs7023329
MTAP
0.790 0.160 9 21816529 intron variant A/G snv 0.50 2
rs801114 0.827 0.120 1 228862088 downstream gene variant T/G snv 0.48 2
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 9
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 2
rs2294008
PSCA ; JRK
0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 3
rs4699052 0.925 0.200 4 103216633 intergenic variant C/T snv 0.44 2
rs13387042
LOC105373874 ; LOC101928278
0.732 0.280 2 217041109 intergenic variant A/G snv 0.44 2
rs13281615
CASC8 ; POU5F1B ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43 2
rs10934853
EEFSEC
0.882 0.160 3 128319530 intron variant C/A snv 0.43 2