Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs564398
CDKN2B-AS1
0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 7
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 6
rs3217992
CDKN2B-AS1 ; CDKN2B
0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 6
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 5
rs523096
CDKN2B-AS1
0.827 0.080 9 22019130 intron variant A/G snv 0.30 5
rs7049105
CDKN2B-AS1
0.807 0.120 9 22028802 intron variant A/G snv 0.58 5
rs7865618
CDKN2B-AS1
0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 5
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs10120688
CDKN2B-AS1
0.807 0.080 9 22056500 intron variant G/A snv 0.50 4
rs10965219
CDKN2B-AS1
0.882 0.080 9 22053688 intron variant A/G snv 0.58 4
rs1063192
CDKN2B ; CDKN2B-AS1
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 4
rs2157719
CDKN2B-AS1
0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 3
rs518394
CDKN2B-AS1
0.827 0.160 9 22019674 intron variant G/C snv 0.30 3
rs643319
CDKN2B-AS1
0.882 0.080 9 22017837 intron variant C/A snv 0.40 3
rs944801
CDKN2B-AS1
0.882 0.120 9 22051671 intron variant G/A;C snv 3
rs12913832
HERC2
0.763 0.200 15 28120472 intron variant A/G snv 0.50 3
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs4656461 0.827 0.040 1 165717968 TF binding site variant G/A snv 0.85 2
rs6475604
CDKN2B-AS1
0.925 0.040 9 22052735 intron variant T/C snv 0.72 2
rs1992314
LOXL1
0.925 0.040 15 73931426 intron variant C/G snv 0.29 2
rs4337252
LOXL1
1.000 0.040 15 73934424 intron variant G/C snv 0.52 2
rs750460
LOXL1
1.000 0.040 15 73949165 intron variant G/A;T snv 2
rs2165241
LOXL1-AS1 ; LOXL1
0.716 0.360 15 73929861 intron variant T/C snv 0.60 2
rs1015213 0.851 0.040 8 51974981 intron variant C/T snv 0.14 1
rs10152898 1.000 0.040 15 73962780 intergenic variant G/A;T snv 1