Disease: Celiac Disease
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 15
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 4
rs1359062
LOC105371664
0.925 0.160 1 192572342 intron variant C/A;G;T snv 2
rs1738074
LOC105378083 ; LOC107986664 ; TAGAP
0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 2