Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17863787
UGT1A9 ; UGT1A8 ; UGT1A6 ; UGT1A7 ; UGT1A10
0.925 0.040 2 233702448 intron variant T/G snv 0.30 9
rs45446698
CYP3A7-CYP3A51P ; CYP3A7 ; ZSCAN25
0.807 0.120 7 99735325 upstream gene variant T/G snv 2.7E-02 9
rs6457374
HLA-B ; LOC112267902
0.851 0.200 6 31304484 intron variant C/T snv 0.81 9
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 9
rs8176693
ABO
0.851 0.160 9 133262254 intron variant C/T snv 9.9E-02 9
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs507666
ABO
1.000 0.040 9 133273983 intron variant A/G snv 8
rs10033900
CFI
0.807 0.040 4 109737911 intron variant T/C snv 0.54 7
rs10399805
CHI3L1
0.851 0.240 1 203186870 upstream gene variant G/A;T snv 7
rs112635299
SERPINA2
1.000 0.040 14 94371805 downstream gene variant G/T snv 1.3E-02 7
rs16893344
CCN4
0.807 0.160 8 133194036 intron variant C/T snv 0.29 7
rs333947
CSF1
1 109928142 intron variant G/A snv 0.13 7
rs6065904
PLTP
1.000 0.080 20 45906012 intron variant G/A snv 0.23 7
rs679574
FUT2 ; LOC105447645
0.827 0.120 19 48702851 intron variant C/G snv 0.45 7
rs11553699
TMEM120B ; RHOF
12 121779004 3 prime UTR variant A/G snv 9.4E-02 6
rs13101828
DGKQ
0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs217181
TXNL4B
16 72080103 intron variant C/T snv 0.20 6
rs2227551
PLAU
0.827 0.120 10 73909432 intron variant G/C;T snv 6
rs2239547
ITIH4
0.882 0.040 3 52821213 intron variant T/C snv 0.27 6
rs2868371
HSPB1
0.827 0.120 7 76301442 upstream gene variant C/G snv 0.22 6
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 6
rs570618
CFH
0.827 0.040 1 196687934 intron variant T/G snv 0.69 6
rs6982502 0.882 0.080 8 125467120 intron variant C/T snv 0.62 6
rs77303550
TXNL4B
16 72045758 intron variant C/T snv 0.19 6
rs1065853 19 44909976 non coding transcript exon variant G/A;C;T snv 5