Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17483466
MIR4435-2HG ; ACOXL
0.827 0.280 2 111039881 intron variant A/G snv 0.15 3
rs7578982
ACOXL ; MIR4435-2HG
2 111078961 intron variant T/C snv 0.27 2
rs6732565
ACOXL
1.000 0.120 2 110850255 intron variant A/G snv 0.38 1
rs4849121
ACOXL
0.925 0.160 2 110842129 intron variant G/A snv 0.44 1
rs13401811
ACOXL
0.925 0.120 2 110858527 intron variant G/A snv 0.19 1
rs4849165
ACOXL
2 110882012 intron variant T/C snv 0.33 1
rs4849162
ACOXL
2 110881658 intron variant T/C snv 0.32 1
rs1439287
ACOXL-AS1 ; ACOXL ; MIR4435-2HG
0.925 0.120 2 111114320 non coding transcript exon variant G/A snv 0.42 1
rs7575878
ACOXL ; MIR4435-2HG
2 111079087 intron variant A/C;T snv 1
rs7599513
ACOXL ; MIR4435-2HG
2 111065699 intron variant A/C snv 0.31 1
rs10207392
ACOXL ; MIR4435-2HG
2 111092082 intron variant A/G snv 0.48 1
rs4849381
MIR4435-2HG ; ACOXL
2 111076804 intron variant G/C snv 0.26 1
rs875063
MIR4435-2HG ; ACOXL
2 111055508 intron variant A/C snv 0.33 1
rs1866493
MIR4435-2HG ; ACOXL
2 111089501 intron variant A/T snv 0.41 1