Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7
rs3130424 0.925 0.040 6 31250462 intergenic variant A/C;G;T snv 5
rs3806156
BTNL2 ; TSBP1-AS1
0.827 0.280 6 32405921 intron variant G/A;T snv 5
rs13091753
LPP
1.000 0.040 3 188396801 intron variant G/C;T snv 2
rs229527
C1QTNF6
0.925 0.160 22 37185445 missense variant C/A;G snv 0.43 2
rs2858870
HLA-DRB1
0.851 0.280 6 32604474 intergenic variant T/A;C snv 2
rs3094061 0.925 0.160 6 30353412 downstream gene variant A/C;T snv 2
rs13118
NEU1
1.000 0.040 6 31859509 3 prime UTR variant A/G;T snv 1
rs13208776
SMOC2
0.882 0.040 6 168540944 intron variant G/A;C snv 1
rs1417210
SLC29A3
0.925 0.040 10 71376162 intron variant G/A;C snv 1
rs1548514 1.000 0.040 6 30419691 downstream gene variant G/A;C;T snv 1
rs17190134
HCG22
1.000 0.040 6 31054083 non coding transcript exon variant C/A;G snv 1
rs2248902 1.000 0.040 6 31266337 downstream gene variant G/A;T snv 1
rs2456973
LOC105369781 ; IKZF4 ; LOC105369780
0.925 0.040 12 56023144 intron variant A/C;G snv 1
rs28383344
LOC107986589 ; HLA-DQA1
1.000 0.040 6 32637290 intron variant C/G;T snv 1
rs2839511
UBASH3A
1.000 0.040 21 42428412 intron variant G/A;T snv 1
rs301819
RERE
0.882 0.120 1 8441726 intron variant A/G;T snv 1
rs3130455
CCHCR1 ; TCF19
1.000 0.040 6 31158201 5 prime UTR variant A/C;T snv 1
rs34101875 1.000 0.040 6 30455581 non coding transcript exon variant G/A;C;T snv 1
rs3823355
HCG9 ; HLA-A
1.000 0.040 6 29974306 upstream gene variant C/A;T snv 1
rs4822024 1.000 0.040 22 41361643 downstream gene variant G/A;C snv 1
rs59374417 0.925 0.040 3 119569567 intergenic variant A/C;T snv 1
rs6902119
FGFR1OP
0.882 0.160 6 167092303 intron variant T/C;G snv 1
rs9261858
MICC
1.000 0.040 6 30416540 non coding transcript exon variant G/A;C snv 1
rs17188127
TRIM15
1.000 0.040 6 30167325 intron variant C/T snv 9.9E-03 1