Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 9
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 6
rs2894207
LINC02571 ; HLA-B
0.882 0.160 6 31295974 intron variant T/C snv 0.20 6
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 5
rs1063192
CDKN2B ; CDKN2B-AS1
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 4
rs31489
CLPTM1L
0.763 0.320 5 1342599 intron variant C/A snv 0.41 4
rs29232 0.925 0.240 6 29643654 intergenic variant C/T snv 0.39 2
rs1572072 1.000 0.120 13 23553071 intergenic variant G/T snv 0.36 1
rs28421666 1.000 0.120 6 32624960 upstream gene variant A/G snv 6.9E-02 1
rs3129055 1.000 0.120 6 29702484 regulatory region variant A/G snv 0.24 1
rs6498114
CIITA ; LOC105371080
1.000 0.080 16 10870261 intron variant G/T snv 0.78 1
rs2517713
HLA-A
1.000 0.120 6 29950322 downstream gene variant G/A;T snv 1
rs2860580
HLA-A
1.000 0.120 6 29938914 upstream gene variant A/C;G;T snv 1
rs189897
ITGA9
1.000 0.120 3 37477054 intron variant T/A snv 0.13 1
rs6774494
MECOM
0.882 0.160 3 169364845 intron variant G/A snv 0.42 1
rs9510787
TNFRSF19
1.000 0.120 13 23631056 intron variant A/G snv 0.20 1