Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 14
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
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 10
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 10
rs17863787
UGT1A9 ; UGT1A8 ; UGT1A6 ; UGT1A7 ; UGT1A10
0.925 0.040 2 233702448 intron variant T/G snv 0.30 7
rs2855812
MICB
0.790 0.360 6 31504943 intron variant G/T snv 0.23 7
rs333947
CSF1
1 109928142 intron variant G/A snv 0.13 7
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 7
rs679574
FUT2 ; LOC105447645
0.827 0.120 19 48702851 intron variant C/G snv 0.45 7
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 7
rs13101828
DGKQ
0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs2227551
PLAU
0.827 0.120 10 73909432 intron variant G/C;T snv 6
rs507666
ABO
1.000 0.040 9 133273983 intron variant A/G snv 6
rs77303550
TXNL4B
16 72045758 intron variant C/T snv 0.19 6
rs10033900
CFI
0.807 0.040 4 109737911 intron variant T/C snv 0.54 5
rs11080055
TMEM97
0.851 0.040 17 28322698 intron variant A/C snv 0.54 5
rs11636952
LMAN1L
15 74821981 intron variant T/C snv 0.48 5
rs13412535
SERPINE2
2 224010157 intron variant G/A snv 0.17 5
rs1410996
CFH
0.807 0.240 1 196727803 intron variant G/A snv 0.46 5
rs570618
CFH
0.827 0.040 1 196687934 intron variant T/G snv 0.69 5
rs62358361
C9
0.851 0.040 5 39327786 intron variant G/C;T snv 5
rs9411378
ABO
9 133270015 intron variant A/C;T snv 5
rs11581607
IL23R
0.925 0.040 1 67242007 intron variant G/A snv 4.6E-02 4