Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 19
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 13
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 11
rs76428106
FLT3
0.851 0.040 13 28029870 intron variant T/C;G snv 10
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 8
rs13138355 4 82624823 upstream gene variant C/A;T snv 4
rs1700159
ACVRL1
1.000 0.040 12 51912002 intron variant C/A;G;T snv 4
rs2239630
CEBPE
0.925 0.160 14 23120140 upstream gene variant A/C;G snv 4
rs45577137
CEBPD
8 47739071 upstream gene variant A/G;T snv 4
rs7288670
GGT5
22 24225858 intron variant A/C;G snv 4
rs10980797
LOC105376219
9 111150273 intron variant A/G;T snv 3
rs113760175
CASC15
6 22343363 intron variant G/A;T snv 3
rs1157008 9 88920798 regulatory region variant T/C;G snv 3
rs11642657 16 85982722 intron variant C/A;T snv 3
rs12151289 19 33260946 intergenic variant G/A;C;T snv 3
rs1991866
CCDC26
8 129611859 intron variant G/A;C snv 3
rs10098310
CCDC26
8 129601368 intron variant G/A;T snv 2
rs10147992
STXBP6
14 25034593 intron variant A/G;T snv 2
rs1021479 16 85923808 upstream gene variant T/A;C snv 2
rs10956483
CCDC26
8 129559864 intron variant G/A;C snv 2
rs112313229 3 46323369 intergenic variant G/A;T snv 2
rs112721625 17 59850066 upstream gene variant TT/-;T;TTT;TTTT delins 2
rs113899791
IRF8
16 85902784 5 prime UTR variant GGCTGCAGGT/-;GGCTGCAGGTGGCTGCAGGT;GGCTGCAGGTGGCTGCAGGTGGCTGCAGGT delins 2