Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs7248668 0.925 0.080 19 39253181 upstream gene variant G/A snv 0.16 3
rs4849133 2 112923864 downstream gene variant C/A;T snv 2
rs3116996 6 33130187 downstream gene variant T/A snv 0.13 1
rs1051861187
ABCB4
0.827 0.080 7 87409385 missense variant A/G snv 6
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs698
ADH1C ; ADH1B
0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs751703423
AIMP2 ; EIF2AK1
7 6023410 missense variant G/A;C snv 1
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs2070666
APOC3
0.882 0.120 11 116830958 intron variant T/A;C snv 4
rs1290547844
BRD4
19 15273041 missense variant C/T snv 4.0E-06 1
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs4804803
CD209
0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs762623
CDKN1A ; DINOL
1.000 0.160 6 36677689 non coding transcript exon variant G/A snv 0.12 2
rs75961395
CFTR
0.763 0.280 7 117509123 missense variant G/A;T snv 4.0E-05 10
rs4950928
CHI3L1
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs2071025
COL11A2
6 33175979 intron variant A/G snv 0.28 0.29 1
rs3811381
CR1
0.763 0.240 1 207616743 missense variant C/A;G snv 8.0E-06; 0.24 11
rs2274567
CR1
0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 10
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs4074
CXCL1
0.827 0.200 4 73870427 intron variant A/G snv 0.46 6
rs868564661
FGFR2
10 121487415 missense variant G/A snv 1
rs954917585
FGFR2
10 121479973 missense variant G/A snv 8.0E-06 1.4E-05 1