Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 9
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 9
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 2
rs7578982
ACOXL ; MIR4435-2HG
2 111078961 intron variant T/C snv 0.27 2
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 2
rs10098310
CCDC26
8 129601368 intron variant G/A;T snv 1
rs10147992
STXBP6
14 25034593 intron variant A/G;T snv 1
rs10956483
CCDC26
8 129559864 intron variant G/A;C snv 1
rs10980800
LOC105376219
9 111153625 intron variant T/C snv 0.21 1
rs12711490 0.925 0.080 16 85939422 intron variant T/C snv 0.18 1
rs1991866
CCDC26
8 129611859 intron variant G/A;C snv 1
rs2292982
IRF8
1.000 0.120 16 85911217 intron variant T/C;G snv 1
rs3731211
CDKN2A
9 21986848 intron variant T/A snv 0.74 1
rs557074
RREB1
1.000 0.040 6 7144958 intron variant T/G snv 0.27 1
rs6584283
LINC01475
0.776 0.080 10 99530544 intron variant T/C snv 0.56 1
rs11611647 12 4224753 intergenic variant T/C snv 0.22 1
rs3095254 6 31253891 intergenic variant C/A;G snv 0.55 1
rs913678 0.882 0.240 20 50338887 regulatory region variant T/C snv 0.51 1
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 3
rs1800973
LYZ
0.827 0.320 12 69350234 missense variant C/A snv 4.2E-02 4.3E-02 1
rs2228468
ACKR2 ; KRBOX1 ; CYP8B1
0.882 0.120 3 42865620 missense variant A/C;T snv 0.43; 8.3E-03 1
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 1
rs12988934
ITGA4
2 181458938 non coding transcript exon variant C/T snv 5.9E-02 1
rs2814778
CADM3-AS1 ; ACKR1
0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 3