Source: GWASCAT

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 61
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 17
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 11
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 11
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 10
rs77542162
ABCA6
1.000 0.040 17 69085137 missense variant A/G snv 9.3E-03 1.0E-02 10
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 10
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 10
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 9
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs2228467
CYP8B1 ; KRBOX1 ; ACKR2
1.000 0.080 3 42864624 missense variant T/C snv 5.1E-02 4.7E-02 8
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 7
rs333947
CSF1
1 109928142 intron variant G/A snv 0.13 7