Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12539316 0.925 0.120 7 73563568 downstream gene variant A/G snv 0.28 5
rs129129
TRIM38
0.925 0.120 6 25960801 upstream gene variant A/G snv 0.73 5
rs13002853
CCDC121 ; GPN1
0.925 0.120 2 27630378 intron variant C/G snv 0.20 5
rs1540276
H4C2
0.925 0.120 6 26028591 upstream gene variant T/A;G snv 5
rs198853
H4C3
0.925 0.120 6 26103868 upstream gene variant T/C snv 0.28 5
rs199726 0.925 0.120 6 25953132 intergenic variant G/A snv 0.73 5
rs199734 0.925 0.120 6 25940165 intergenic variant G/A;C snv 5
rs199736 0.925 0.120 6 25936559 intergenic variant C/T snv 0.72 5
rs199737 0.925 0.120 6 25933310 upstream gene variant A/C;T snv 5
rs199739 0.925 0.120 6 25960281 upstream gene variant A/C;G snv 0.78 5
rs199751 0.925 0.120 6 26015355 upstream gene variant T/C snv 0.77 5
rs199752 0.925 0.120 6 26012647 upstream gene variant C/T snv 0.77 5
rs199753 0.925 0.120 6 26001660 non coding transcript exon variant G/A snv 0.77 5
rs2030746
LOC105373585
0.925 0.120 2 120551912 downstream gene variant C/T snv 0.44 5
rs2286276
TBL2
0.925 0.120 7 73573024 non coding transcript exon variant C/T snv 0.28 5
rs2384656
ZNF512
0.925 0.120 2 27609188 intron variant A/G snv 0.27 5
rs2794719
LOC108783645 ; HFE
0.925 0.120 6 26088662 intron variant T/C;G snv 5
rs35385468 0.925 0.120 6 26101212 upstream gene variant -/C delins 9.7E-03 5
rs386406569 0.925 0.120 6 26101212 upstream gene variant -/C delins 5
rs4401650
H2AC4
0.925 0.120 6 26034980 upstream gene variant G/A snv 0.75 5
rs442601 0.925 0.120 6 25934296 upstream gene variant G/A snv 0.72 5
rs4481233
SLC2A9
0.925 0.120 4 9954455 intron variant C/T snv 0.16 5
rs4665382
C2orf16
0.925 0.120 2 27560934 intron variant T/C snv 0.23 5
rs4665383
C2orf16
0.925 0.120 2 27568688 synonymous variant C/G snv 0.24 5
rs4665987 0.925 0.120 2 27532958 upstream gene variant G/A;T snv 5