Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs530960
FRK
6 116078089 intergenic variant A/G snv 0.99 1
rs2973662
TENM2
5 167783467 intron variant A/G snv 0.98 1
rs1291621
SCAF11
1.000 0.040 12 45947038 intron variant A/G snv 0.98 1
rs3850930
TRIM51CP
1.000 0.080 11 48948392 non coding transcript exon variant A/G snv 0.98 1
rs524772 3 150729892 downstream gene variant G/A snv 0.98 2
rs1146075
LOC105371954 ; LINC00470
18 1366300 non coding transcript exon variant C/T snv 0.98 1
rs294227 1 22691071 regulatory region variant A/C snv 0.98 1
rs1225764
SYCP2L
0.925 0.040 6 10924759 intron variant A/G;T snv 0.98 2
rs1039049
CFAP299
1.000 0.040 4 80416472 intron variant G/A snv 0.98 1
rs2139709
LINC00882
0.925 0.040 3 106780512 intron variant A/G snv 0.98 2
rs428595
LOC107985532
1.000 0.120 22 21662102 non coding transcript exon variant A/G snv 0.98 3
rs11475465
MMP24OS ; MMP24-AS1-EDEM2
20 35223007 intron variant A/- delins 0.98 1
rs1784848 18 2176439 intron variant T/C snv 0.98 1
rs10862344
PPFIA2
1.000 0.040 12 81697021 intron variant A/C snv 0.98 1
rs4562194
LOC105375322
0.925 0.040 7 64300980 upstream gene variant C/G snv 0.98 2
rs6511404
ZNF730
1.000 0.040 19 23105059 intron variant G/A snv 0.98 1
rs7507433
ZNF730
1.000 0.040 19 23121779 intron variant G/A snv 0.98 1
rs2446597
FRMD4A
1.000 0.040 10 14007605 intron variant A/G snv 0.98 1
rs1562263
LUZP2
0.925 0.040 11 25080410 3 prime UTR variant C/T snv 0.98 2
rs1942462
NETO1
0.925 0.040 18 72842589 intron variant C/T snv 0.98 2
rs4486987
ARHGAP28
1.000 0.040 18 6762371 intron variant G/A snv 0.98 1
rs330033 1.000 0.040 8 9243439 intron variant G/A snv 0.98 1
rs2255280
C9 ; DAB2
0.925 0.120 5 39394887 intron variant C/A snv 0.98 1
rs9840264
FOXP1
1.000 0.040 3 71141552 intron variant G/A snv 0.98 1
rs692885 0.925 0.040 15 49757229 intergenic variant G/T snv 0.98 2