Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs17145750
MLXIPL
0.925 0.120 7 73612048 intron variant C/A;T snv 7
rs13022873
ZNF512
0.882 0.120 2 27592643 intron variant A/C;T snv 6
rs4666002
ZNF512
0.925 0.120 2 27617773 intron variant G/A;C snv 6
rs115810
TRIM38
0.925 0.120 6 25975655 intron variant G/A;C snv 5
rs11983997 0.925 0.120 7 73524914 upstream gene variant G/A;C snv 5
rs1540276
H4C2
0.925 0.120 6 26028591 upstream gene variant T/A;G snv 5
rs199734 0.925 0.120 6 25940165 intergenic variant G/A;C snv 5
rs199737 0.925 0.120 6 25933310 upstream gene variant A/C;T snv 5
rs2794719
LOC108783645 ; HFE
0.925 0.120 6 26088662 intron variant T/C;G snv 5
rs386406569 0.925 0.120 6 26101212 upstream gene variant -/C delins 5
rs4665987 0.925 0.120 2 27532958 upstream gene variant G/A;T snv 5
rs6760250
ZNF512
0.925 0.120 2 27589385 intron variant G/A;C snv 5
rs807212 0.925 0.120 6 26065393 regulatory region variant A/G;T snv 5
rs9379818 0.925 0.120 6 26022978 downstream gene variant G/A;T snv 5
rs10946785
CARMIL1
0.925 0.120 6 25616840 intron variant G/A;T snv 4
rs1165151
SLC17A1
0.925 0.120 6 25821388 intron variant T/A;G snv 4
rs1165152
SLC17A1
0.925 0.120 6 25818538 intron variant A/C;G;T snv 4
rs1165153
SLC17A1
0.925 0.120 6 25817561 intron variant A/G;T snv 4
rs1165205
SLC17A3
0.925 0.120 6 25870314 intron variant T/A;G snv 4
rs1184804
SLC17A3
0.925 0.120 6 25867998 intron variant T/A;C snv 4
rs1185567
SLC17A1
0.925 0.120 6 25818360 intron variant A/G;T snv 4
rs12215823
H2BC1 ; H2AC1 ; SLC17A1
0.925 0.120 6 25725846 upstream gene variant G/C;T snv 4
rs13023194 0.925 0.120 2 27744393 intergenic variant G/A;C snv 4
rs1436306 0.925 0.120 6 25948193 intergenic variant A/G;T snv 4