Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12661667
USP49
6 41824807 intron variant C/T snv 0.20 4
rs7753507
USP49
6 41816356 intron variant C/T snv 0.52 3
rs6899876
USP49
6 41829232 intron variant T/C;G snv 0.23 3
rs8393
TOMM6 ; USP49
6 41790098 3 prime UTR variant C/A snv 0.56 2
rs2254805
USP49
6 41878372 intron variant T/A;G snv 2
rs11753329
USP49
6 41820642 intron variant T/G snv 0.14 2
rs2488338
USP49
6 41840613 intron variant A/G snv 0.44 2
rs2153878
USP49
6 41805584 intron variant G/A snv 0.16 0.15 2
rs9357366
USP49
6 41819238 intron variant T/G snv 0.20 2
rs9381096
USP49
6 41853399 intron variant G/A snv 0.16 2
rs9381094
USP49
6 41832891 non coding transcript exon variant T/C;G snv 0.19 2
rs2249703
USP49
6 41847022 intron variant A/G snv 0.51 2
rs9369312
USP49
6 41873797 intron variant A/T snv 0.19 2
rs2251084
USP49
6 41870381 intron variant T/A;C snv 2
rs1887718
USP49
6 41889953 intron variant C/T snv 0.49 2
rs2025951
USP49
6 41859455 intron variant A/G snv 0.49 2
rs2185798
USP49
6 41805838 synonymous variant G/A;C snv 4.0E-06; 0.54 2
rs9394834
USP49
6 41839055 intron variant G/A snv 0.19 2
rs9381097
USP49
6 41880062 intron variant G/A snv 0.19 2
rs2253961
USP49
6 41859273 intron variant A/G snv 0.44 2
rs1891453
USP49
6 41797527 intron variant T/C snv 0.19 2
rs2254474
USP49
6 41875306 intron variant T/A;G snv 2
rs6902650
USP49
6 41796342 3 prime UTR variant G/A snv 0.54 2
rs9367112
USP49
6 41802182 intron variant T/C snv 0.19 2
rs3747750
USP49
6 41792634 3 prime UTR variant C/G snv 0.19 2