Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 7
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 5
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs3134603
PPT2-EGFL8 ; PPT2
0.851 0.360 6 32158225 non coding transcript exon variant A/C;G;T snv 4
rs6457327 0.790 0.320 6 31106253 downstream gene variant A/C snv 0.66 3
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 3
rs2151280
CDKN2B-AS1
0.701 0.360 9 22034720 non coding transcript exon variant G/A snv 0.46 3
rs872071
IRF4
0.742 0.360 6 411064 3 prime UTR variant A/G;T snv 3
rs3774372
ULK4
1.000 0.160 3 41835922 missense variant T/C snv 0.17 0.18 3
rs9815354
ULK4
0.925 0.160 3 41871159 intron variant G/A;T snv 3
rs12630450 1.000 0.160 3 169762416 downstream gene variant A/G snv 0.33 2
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 2
rs7633750 1.000 0.160 3 169791456 upstream gene variant G/A snv 0.38 2
rs2456449
CASC19 ; PCAT1
0.827 0.280 8 127180736 intron variant A/G snv 0.30 2
rs2235544
DIO1
0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 2
rs1050976
IRF4
0.851 0.280 6 408079 3 prime UTR variant C/T snv 0.37 2
rs12621278
ITGA6
0.790 0.280 2 172446825 intron variant A/G snv 4.9E-02 2
rs6465657
LMTK2
0.807 0.280 7 98187015 intron variant C/T snv 0.41 0.37 2
rs10936601
LRRC34
1.000 0.160 3 169810661 intron variant C/T snv 0.37 2
rs1317082
MYNN
0.882 0.200 3 169779797 non coding transcript exon variant A/G snv 0.21 2