Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2294882
TSBP1-AS1 ; BTNL2
6 32399738 intron variant T/C snv 0.19 2
rs10885
PRRC2A
6 31636814 missense variant C/T snv 0.14 0.17 1
rs200688486 6 32621223 regulatory region variant -/T delins 1
rs204992
PBX2
6 32189131 intron variant G/A snv 0.22 1
rs2294884
TSBP1-AS1 ; BTNL2
6 32399482 intron variant T/A;G snv 0.18 1
rs28362680
BTNL2 ; TSBP1-AS1
6 32403039 missense variant G/A snv 0.14 0.12 1
rs3104369
HLA-DQA1
6 32634705 intron variant T/C snv 0.71 1
rs3130070
PRRC2A
6 31624031 intron variant A/G snv 0.17 1
rs3130623
PRRC2A
6 31629923 intron variant C/T snv 0.18 1
rs9267536
LOC105375019 ; LY6G5C
6 31683417 intron variant A/C snv 5.3E-02 1
rs9271488 6 32621223 regulatory region variant G/T snv 0.27 1
rs9368726
HLA-DRB9
6 32470765 intron variant T/C snv 0.29 1
rs9405108
HLA-DRB9
6 32470871 intron variant C/T snv 0.29 1
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 1
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 8
rs2516049
HLA-DRB1
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 9
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs652888
EHMT2-AS1 ; EHMT2 ; LOC107986588 ; CYP21A2
0.776 0.480 6 31883457 non coding transcript exon variant A/G snv 0.18 0.20 6
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 8
rs477515
HLA-DRB1
0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 7
rs3115663
PRRC2A ; MIR6832
0.827 0.360 6 31634066 non coding transcript exon variant T/C snv 0.17 6
rs3130618
CSNK2B ; GPANK1
0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 6
rs7194
HLA-DRA
0.827 0.280 6 32444703 3 prime UTR variant G/A snv 0.61 5
rs7192
HLA-DRA
0.827 0.200 6 32443869 missense variant T/G snv 0.64 0.61 3
rs11229
PRRC2A
0.851 0.280 6 31635993 synonymous variant A/G snv 0.14 0.17 6