Disease: Primary biliary cirrhosis
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs694739
LOC102723878
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 6
rs7665090
MANBA
0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 4
rs1800693
TNFRSF1A
0.776 0.360 12 6330843 non coding transcript exon variant T/C snv 0.36; 4.0E-06 0.38 3
rs2293370
TIMMDC1
0.882 0.160 3 119501087 intron variant G/A snv 0.18 3
rs2546890
LOC285626
0.882 0.200 5 159332892 non coding transcript exon variant A/G snv 0.52 3
rs2300747
MIR548AC ; CD58
0.882 0.200 1 116561593 intron variant A/G snv 0.19 2
rs6897932
IL7R
0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 2