Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2308321
MGMT
0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 29
rs1223231582
PRSS1
0.677 0.280 7 142750639 missense variant A/G snv 7.0E-06 24
rs1049074086
CTSD
0.925 0.120 11 1759567 missense variant A/G snv 7.0E-06 9
rs11039149
NR1H3
0.827 0.280 11 47255124 intron variant A/G snv 0.19 6
rs9564966 0.851 0.120 13 73322084 intergenic variant A/G snv 0.52 4
rs1209809979
AKR1A1
0.925 0.120 1 45568989 missense variant A/G snv 4.0E-06 3
rs2027605
BACH1
1.000 0.120 21 29354452 intron variant A/G snv 0.48 3
rs4269383
LOC105378072 ; LOC101928923
0.882 0.120 6 155876368 intergenic variant A/G snv 0.37 3
rs4619
IGFBP1
0.882 0.160 7 45893070 missense variant A/G snv 0.36 0.38 3
rs11085754
SMARCA4
0.925 0.120 19 11017920 intron variant A/G snv 0.41 2
rs12456874
LDLRAD4
0.925 0.120 18 13366863 intron variant A/G snv 0.20 2
rs1318
LOC101928045 ; PITPNC1
0.925 0.120 17 67695266 3 prime UTR variant A/G snv 0.30 2
rs138147246
OGG1
0.925 0.120 3 9756551 synonymous variant A/G snv 8.0E-06 1.4E-05 2
rs1455311
LINC01088
0.925 0.160 4 79043433 intron variant A/G snv 0.14 2
rs1547374
LOC105372815
0.925 0.120 21 42358786 downstream gene variant A/G snv 0.32 2
rs1810205
CUBN
0.925 0.120 10 16923228 intron variant A/G snv 0.47 2
rs371609024
FUT8
0.925 0.120 14 65629530 missense variant A/G snv 4.0E-06 2
rs4149086
SLCO1B1
0.925 0.120 12 21239517 3 prime UTR variant A/G snv 4.5E-04 2
rs4795218
HNF1B ; LOC105371754
0.925 0.120 17 37718512 intron variant A/G snv 0.82 2
rs5768709
TAFA5
0.925 0.120 22 48533757 intron variant A/G snv 0.36 2
rs708224
BICD1
0.925 0.120 12 32283475 intron variant A/G snv 0.50 2
rs747601652
CRYZ
0.925 0.120 1 74723233 missense variant A/G snv 1.2E-05 2
rs935821839
TP73
0.925 0.120 1 3727199 missense variant A/G snv 7.0E-06 2
rs2832290
BACH1
1.000 0.120 21 29356542 intron variant A/G snv 0.48 1
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115