Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 7
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 7
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 5
rs9272535
HLA-DQA2 ; LOC107986589 ; HLA-DQA1
0.827 0.280 6 32638979 synonymous variant G/A snv 3.0E-05 1.8E-03 5
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 5
rs301
LPL
0.925 0.160 8 19959423 intron variant T/C snv 0.24 0.26 5
rs735665
GRAMD1B
0.776 0.280 11 123490689 intron variant G/A snv 0.15 4
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 4
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 4
rs926070
TSBP1-AS1 ; TSBP1
0.827 0.320 6 32289789 intron variant G/A snv 0.68 4
rs305061 0.851 0.280 16 85942053 intron variant C/A;T snv 3
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 3
rs7176508
DRAIC
0.851 0.280 15 69726651 intron variant A/G snv 0.67 3
rs9273363
HLA-DQB1-AS1
0.851 0.280 6 32658495 upstream gene variant C/A snv 0.23 3
rs872071
IRF4
0.742 0.360 6 411064 3 prime UTR variant A/G;T snv 3
rs13702
LPL
0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv 3
rs17483466
MIR4435-2HG ; ACOXL
0.827 0.280 2 111039881 intron variant A/G snv 0.15 3
rs11755724
RREB1
0.807 0.320 6 7118757 intron variant A/G;T snv 3
rs13397985
SP110 ; SP140
0.827 0.280 2 230226508 intron variant T/C;G snv 3
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 2
rs7169431 0.925 0.200 15 56048698 intergenic variant A/G;T snv 2
rs9378805 0.851 0.280 6 417727 intergenic variant A/C snv 0.36 2
rs210134
BAK1 ; GGNBP1
1.000 0.120 6 33572432 intron variant A/G snv 0.72 2
rs2456449
CASC19 ; PCAT1
0.827 0.280 8 127180736 intron variant A/G snv 0.30 2