Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs3811647
TF
0.807 0.120 3 133765185 intron variant G/A snv 0.31 10
rs174577
FADS2
1.000 0.080 11 61837342 intron variant C/A snv 0.38 9
rs744653 2 189514024 regulatory region variant C/T snv 0.84 4
rs8177240
TF
3 133758857 intron variant T/C;G snv 0.29 4
rs9990333 3 196100334 intergenic variant C/T snv 0.42 3
rs6486121
ARNTL
11 13334223 intron variant C/T snv 0.53 3
rs4921915 8 18414956 intergenic variant G/A snv 0.71 2
rs8177179
INHCAP ; TF
0.925 0.080 3 133744613 intron variant G/A snv 0.58 2