Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 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
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
rs12913832
HERC2
0.763 0.200 15 28120472 intron variant A/G snv 0.50 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
rs1992314
LOXL1
0.925 0.040 15 73931426 intron variant C/G snv 0.29 2
rs2165241
LOXL1-AS1 ; LOXL1
0.716 0.360 15 73929861 intron variant T/C snv 0.60 2
rs4337252
LOXL1
1.000 0.040 15 73934424 intron variant G/C snv 0.52 2
rs6475604
CDKN2B-AS1
0.925 0.040 9 22052735 intron variant T/C snv 0.72 2
rs750460
LOXL1
1.000 0.040 15 73949165 intron variant G/A;T snv 2
rs10038177
WDR36
0.925 0.040 5 111100751 intron variant C/T snv 0.53 0.54 1
rs1015213 0.851 0.040 8 51974981 intron variant C/T snv 0.14 1
rs11024102
PLEKHA7
0.851 0.040 11 16987058 intron variant T/C snv 0.20 1
rs11656696
GAS7
0.882 0.040 17 10130362 intron variant C/A snv 0.36 1
rs12150284
GAS7
1.000 0.040 17 10127773 intron variant C/A;G;T snv 1
rs12440667
LOXL1
1.000 0.040 15 73939098 intron variant C/A;T snv 1
rs1256031
ESR2
0.790 0.200 14 64279461 intron variant G/A;T snv 0.57 1
rs2028386
LOXL1
1.000 0.040 15 73934367 intron variant C/A;G snv 1
rs2093210
C14orf39
1.000 0.040 14 60490561 intron variant C/T snv 0.45 1
rs2304719
LOXL1
1.000 0.040 15 73943159 intron variant C/T snv 0.30 1