Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1569414
FAM118A
0.807 0.160 22 45331684 intron variant T/G snv 0.44 6
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 6
rs2024092
SBNO2
0.827 0.120 19 1124032 intron variant G/A snv 0.24 0.26 6
rs2143178 0.827 0.120 22 39264824 intron variant T/C snv 0.19 6
rs2227551
PLAU
0.827 0.120 10 73909432 intron variant G/C;T snv 6
rs2266961
UBE2L3
0.807 0.160 22 21574308 intron variant C/G snv 0.18 6
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69 6
rs2451258
LOC112267968
0.807 0.160 6 159085568 intron variant C/T snv 0.75 6
rs259964
ZNF831
0.827 0.120 20 59249254 intron variant A/G;T snv 6
rs26528
IL27
0.807 0.200 16 28506388 intron variant T/C snv 0.43 6
rs2812378
CCL21
0.790 0.200 9 34710263 intron variant G/A;C snv 6
rs2816958
NR5A2
0.827 0.120 1 200132792 intron variant A/G snv 0.84 6
rs28998802
NOS2
0.807 0.120 17 27797882 intron variant G/A snv 0.11 6
rs34779708
CREM
0.827 0.120 10 35177257 intron variant T/G snv 0.33 6
rs367569
LOC105371082 ; RMI2
0.807 0.120 16 11271643 intron variant C/T snv 0.32 6
rs3766606
PARK7
0.827 0.120 1 7962137 intron variant G/T snv 0.22 6
rs3776414
DAP
0.827 0.120 5 10689450 intron variant T/G snv 0.48 6
rs3853824
C17orf67
0.827 0.120 17 56803632 intron variant T/C snv 0.66 6
rs395157
OSMR
0.827 0.120 5 38867630 intron variant C/T snv 0.47 6
rs4561177
RDX ; ZC3H12C
0.807 0.120 11 110091706 intron variant A/G snv 0.36 6
rs4921482
LOC285626
0.807 0.120 5 159337470 intron variant T/C;G snv 6
rs4946717
PRDM1
0.827 0.120 6 106026874 intron variant C/A;G;T snv 6
rs56167332 0.807 0.160 5 159400761 intron variant C/A;T snv 6
rs6062496
TNFRSF6B ; RTEL1-TNFRSF6B
0.827 0.120 20 63697746 intron variant G/A snv 0.52 6
rs6863411
NDFIP1
0.827 0.120 5 142133639 intron variant A/T snv 0.67 6