Disease: Pemphigus Vulgaris
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2516049
HLA-DRB1
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 9
rs660895
HLA-DRB1
0.752 0.360 6 32609603 intergenic variant A/G snv 0.19 6
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs2395157
TSBP1-AS1
0.827 0.240 6 32380368 intron variant A/G snv 0.24 5
rs2858331 0.827 0.240 6 32713500 upstream gene variant A/G snv 0.42 5
rs3892710 0.851 0.240 6 32715085 upstream gene variant C/T snv 0.22 4
rs12660382
HCP5
0.882 0.200 6 31475546 intron variant C/T snv 0.19 3
rs2244839
HCP5 ; HCG26
0.882 0.200 6 31470591 non coding transcript exon variant G/A;T snv 3
rs2395488
HCP5
0.882 0.160 6 31478132 non coding transcript exon variant A/G snv 0.34 3
rs9268542 0.851 0.280 6 32416944 intergenic variant A/G snv 0.35 3
rs9275184 0.882 0.200 6 32686937 regulatory region variant T/C snv 9.1E-02 3
rs1980495
TSBP1-AS1
0.925 0.160 6 32379017 intron variant A/C snv 0.24 2
rs2246618
MICB
0.882 0.160 6 31511209 upstream gene variant C/T snv 0.32 2
rs2516424
MICB-DT
0.925 0.160 6 31480538 non coding transcript exon variant A/G snv 0.34 2