Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs139016349
MRAS
1.000 0.040 3 138380319 intron variant -/CTT delins 0.21 1
rs34091558
LMOD1
1.000 0.040 1 201917642 intron variant A/- delins 0.25 1
rs528732638
CHST9 ; AQP4-AS1
0.851 0.120 18 26940224 intron variant A/-;AA;AAA;AAAA delins 2
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 7
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs55791371
SMARCA4
0.925 0.080 19 11077477 intron variant A/C snv 0.11 3
rs606452
SERPINH1
1.000 0.040 11 75565133 intron variant A/C snv 0.78 3
rs12315434
R3HDM2
1.000 0.040 12 57387153 intron variant A/C snv 0.16 2
rs2128739 0.925 0.080 11 103802549 intron variant A/C snv 0.68 2
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 2
rs4932373
FES
1.000 0.040 15 90886057 intron variant A/C snv 0.25 2
rs11057840
SCARB1
1.000 0.040 12 124831509 intron variant A/C snv 0.16 1
rs11072811
MORF4L1
1.000 0.040 15 78839988 intron variant A/C snv 0.51 1
rs13118820
LOC105377505
1.000 0.040 4 155515365 intron variant A/C snv 0.63 1
rs145099029 1.000 0.040 6 160871806 downstream gene variant A/C snv 2.6E-03 1
rs1476098
BCAS3
1.000 0.040 17 61159652 intron variant A/C snv 0.66 1
rs1807214 1.000 0.040 15 89022026 regulatory region variant A/C snv 0.29 1
rs2239704
LTA ; LOC100287329
0.732 0.320 6 31572364 5 prime UTR variant A/C snv 0.64 1
rs2738447
LDLR
1.000 0.040 19 11116804 intron variant A/C snv 0.65 1
rs2965169
BCL3
0.925 0.120 19 44747899 non coding transcript exon variant A/C snv 0.50 1
rs4613862
LINC02542
1.000 0.040 6 81902554 intron variant A/C snv 0.37 1
rs4644046 1.000 0.040 6 51520211 intergenic variant A/C snv 0.38 1
rs56170783
PLPP3
1.000 0.040 1 56550459 intron variant A/C snv 6.5E-02 1
rs585967 1.000 0.040 2 21047682 upstream gene variant A/C snv 0.81 1
rs6740322
THADA
1.000 0.040 2 43334790 intron variant A/C snv 0.20 1