Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2239647
AKAP6
0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65 4
rs17245822 13 72557556 intergenic variant A/C snv 0.34 2
rs2163503
ZRANB2-AS2
1 71335356 intron variant A/C snv 0.17 2
rs6492538 13 91341492 intergenic variant A/C snv 0.83 2
rs750472
PPP1R16A ; FOXH1
8 144476070 upstream gene variant A/C snv 0.50 2
rs10057590
LINC02240
5 124999554 intron variant A/C snv 0.62 1
rs10171320
LOC101928273
2 137928042 intergenic variant A/C snv 0.62 1
rs10400054
SORCS3
10 105004435 intron variant A/C snv 0.24 1
rs10510388
LMCD1-AS1
3 8215887 intron variant A/C snv 0.28 1
rs11257952
CAMK1D
10 12714714 intron variant A/C snv 0.36 1
rs1157684 4 133651129 intergenic variant A/C snv 0.31 1
rs117269860
SLC25A17
22 40790485 intron variant A/C snv 2.1E-02 1
rs11904541
LOC105374820
2 78546010 intergenic variant A/C snv 0.40 1
rs12376674
LOC105376097
9 78872110 TF binding site variant A/C snv 0.10 1
rs12739596 1 165390877 intergenic variant A/C snv 0.18 1
rs12997235
MAPRE3 ; MAPRE3-AS1
2 27006211 intron variant A/C snv 0.36 1
rs17748359 8 92278935 intergenic variant A/C snv 0.21 1
rs1993408
LOC107986022
3 117892638 intron variant A/C snv 0.36 1
rs2164552 3 143969456 upstream gene variant A/C snv 0.56 1
rs2169642 3 82688622 intergenic variant A/C snv 0.34 1
rs2358628
LIN52
14 74165054 intron variant A/C snv 0.57 1
rs2806934 13 53069972 intergenic variant A/C snv 0.44 1
rs2920861
RTN4
2 55090980 intron variant A/C snv 0.92 1
rs2962438
LOC102723560
16 62744695 intergenic variant A/C snv 0.86 1
rs317056 4 35430215 intergenic variant A/C snv 0.48 1