Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs200688486 6 32621223 regulatory region variant -/T delins 1
rs12154141 6 62460168 downstream gene variant A/C snv 0.20 1
rs9267536
LOC105375019 ; LY6G5C
6 31683417 intron variant A/C snv 5.3E-02 1
rs28366298
HLA-DRB1
0.925 0.120 6 32593082 upstream gene variant A/C;T snv 3
rs8084
HLA-DRA
1.000 0.120 6 32443258 splice acceptor variant A/C;T snv 0.61; 8.1E-06 2
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs652888
EHMT2-AS1 ; EHMT2 ; LOC107986588 ; CYP21A2
0.776 0.480 6 31883457 non coding transcript exon variant A/G snv 0.18 0.20 10
rs11229
PRRC2A
0.851 0.280 6 31635993 synonymous variant A/G snv 0.14 0.17 6
rs3117583
APOM ; BAG6
0.925 0.200 6 31651799 5 prime UTR variant A/G snv 0.14 0.17 3
rs204995
PBX2
1.000 0.120 6 32186508 non coding transcript exon variant A/G snv 0.21 0.27 2
rs2213586
HLA-DRA
1.000 0.040 6 32445317 downstream gene variant A/G snv 0.61 2
rs3130626
PRRC2A
1.000 0.120 6 31630712 synonymous variant A/G snv 0.15 0.17 2
rs7195
HLA-DRA
1.000 0.040 6 32444762 3 prime UTR variant A/G snv 0.61 2
rs3130070
PRRC2A
6 31624031 intron variant A/G snv 0.17 1
rs2736157
MIR6832 ; PRRC2A
1.000 0.120 6 31633043 intron variant A/G;T snv 0.15 0.17 2
rs2854275
HLA-DQB1 ; HLA-DQB1-AS1
0.925 0.120 6 32660651 non coding transcript exon variant C/A snv 9.6E-02 4
rs2239802
HLA-DRA
0.882 0.200 6 32444069 intron variant C/A;G;T snv 4
rs3130618
CSNK2B ; GPANK1
0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 7
rs2239803
HLA-DRA
0.882 0.240 6 32444056 intron variant C/A;T snv 0.50 4
rs4919510
SEMA4G ; MIR608 ; MRPL43
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs204994
PBX2
0.925 0.120 6 32187221 non coding transcript exon variant C/T snv 0.18 0.21 4
rs10947262
TSBP1-AS1 ; BTNL2
0.925 0.040 6 32405535 non coding transcript exon variant C/T snv 0.12 3
rs7754768 1.000 0.040 6 32452402 regulatory region variant C/T snv 0.56 2
rs9267532
LY6G5B ; CSNK2B
1.000 0.120 6 31672202 missense variant C/T snv 7.4E-02 7.9E-02 2