Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4271113 1.000 0.080 X 34874386 regulatory region variant G/A snv 0.14 1
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 8
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 4
rs743777
IL2RB
0.827 0.200 22 37155567 intron variant A/G snv 0.36 4
rs229541
C1QTNF6
0.807 0.200 22 37195278 intron variant G/A snv 0.49 2
rs2412973
HORMAD2
1.000 0.080 22 30133642 intron variant C/A snv 0.54 2
rs5753037
HORMAD2 ; LOC105372988
0.925 0.160 22 30185733 intron variant C/A;T snv 2
rs5771069
IL17REL
0.925 0.120 22 49997051 missense variant A/G snv 0.56 0.55 2
rs2283792
MAPK1
1.000 0.080 22 21776836 intron variant T/G snv 0.54 1
rs4819388
ICOSLG
0.790 0.240 21 44227538 3 prime UTR variant T/C snv 5
rs1736135
LOC101927745
0.851 0.160 21 15432901 intron variant T/C snv 0.33 4
rs2836878 0.851 0.200 21 39093608 intergenic variant G/A snv 0.23 4
rs762421
GATD3A
0.851 0.360 21 44195678 intron variant G/A snv 3
rs9976767
UBASH3A
0.882 0.200 21 42416281 intron variant A/G snv 0.45 2
rs1569723 0.851 0.280 20 46113425 upstream gene variant C/A snv 0.80 4
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 4
rs1799990
PRNP
0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 2
rs2281808
SIRPG
0.925 0.160 20 1629905 intron variant T/A;C snv 2
rs2315008
ZGPAT
0.925 0.120 20 63712604 intron variant T/G snv 0.70 2
rs495337
SPATA2
0.925 0.120 20 49905793 synonymous variant G/A snv 0.44 0.35 2
rs6017342
LINC01620
0.925 0.120 20 44436388 non coding transcript exon variant A/C snv 0.62 2
rs6074022 0.851 0.240 20 46111557 TF binding site variant C/G;T snv 2
rs2248359
CYP24A1
0.790 0.400 20 54174979 upstream gene variant C/T snv 0.47 1
rs2425752
NCOA5
0.851 0.160 20 46073481 intron variant T/C snv 0.79 1
rs2762932
CYP24A1
0.882 0.200 20 54151852 downstream gene variant T/C snv 0.17 1