Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 9
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 6
rs9788721
HYKK
1.000 0.040 15 78510527 intron variant C/T snv 0.65 6
rs1045241
TNFAIP8
1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 5
rs138544659
CHRNA3
1.000 0.040 15 78608359 intron variant T/G snv 0.28 5
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 5
rs3786897
PEPD
1.000 0.080 19 33402102 intron variant A/G snv 0.45 5
rs55958997
CHRNB4
1.000 0.040 15 78623530 upstream gene variant C/A snv 0.32 5
rs979012 1.000 0.080 20 6642727 intergenic variant T/C snv 0.67 5
rs4886782
LOXL1
1.000 0.040 15 73936469 intron variant G/A snv 0.27 4
rs798502
AMZ1 ; GNA12
1.000 0.040 7 2750246 intron variant A/C;G snv 4
rs8031948
HYKK
1.000 0.040 15 78523715 intron variant G/T snv 0.27 4
rs11205277 1.000 0.120 1 149920979 upstream gene variant A/C;G;T snv 3
rs12459249 1.000 0.040 19 40833991 intron variant T/C snv 0.66 3
rs12692738
COBLL1
1.000 0.080 2 164701742 intron variant T/C snv 0.34 3
rs17484524
IREB2
1.000 0.040 15 78480334 intron variant A/G snv 0.23 3
rs17487223
CHRNB4
1.000 0.040 15 78631645 intron variant C/T snv 0.27 3
rs2009746
IREB2
1.000 0.040 15 78461760 intron variant A/G snv 0.29 3
rs2656065
IREB2
1.000 0.040 15 78458207 intron variant G/A snv 0.39 3
rs7180002
CHRNA5
1.000 0.040 15 78581651 intron variant A/T snv 0.26 3
rs7181486
IREB2
1.000 0.040 15 78449276 intron variant T/C snv 0.29 3
rs7773004 1.000 0.040 6 26267527 downstream gene variant A/C;G;T snv 3
rs8042238
IREB2
1.000 0.040 15 78481929 intron variant C/T snv 0.51 3
rs1049281
HLA-C
1.000 0.120 6 31268790 3 prime UTR variant T/C snv 0.68 2