Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs149104283
SLCO1B3-SLCO1B7
0.882 0.040 12 20930928 intron variant C/G;T snv 4
rs1050274678
SLC19A1
0.925 0.040 21 45530803 missense variant C/T snv 1.1E-05 7.0E-06 3
rs1453542
OR4D6
0.925 0.040 11 59457412 missense variant G/A;C snv 7.2E-05; 0.26 3
rs17376848
DPYD
0.925 0.040 1 97450068 synonymous variant A/G snv 5.1E-02 4.3E-02 3
rs3758581
CYP2C19
0.925 0.040 10 94842866 missense variant A/G snv 0.95 3
rs4150558
GTF2H1
0.882 0.040 11 18332808 non coding transcript exon variant T/A snv 8.7E-03 3
rs45547640
XDH
0.925 0.040 2 31346794 missense variant T/G snv 2.0E-03 6.5E-04 3
rs5925720
DDX53 ; PTCHD1-AS
0.925 0.040 X 23001200 missense variant G/T snv 0.15 9.4E-02 3
rs72552763
SLC22A1
0.925 0.040 6 160139849 inframe deletion GAT/- delins 0.15 3
rs775729712
DCTD
0.925 0.040 4 182915501 missense variant G/C snv 3
rs10824095
ADK
0.925 0.040 10 74176853 5 prime UTR variant C/G;T snv 0.67 2
rs11719165 0.925 0.040 3 194865359 intergenic variant T/C snv 0.53 2
rs117506642
LOC105376755
1.000 0.040 2 195143585 intergenic variant C/A;T snv 2
rs117829974 1.000 0.040 3 62886233 intergenic variant C/A;G;T snv 2
rs12046844 0.925 0.040 1 65772696 regulatory region variant G/A snv 0.17 2
rs1260186456
ABCC1
0.925 0.040 16 16102659 missense variant G/T snv 9.4E-06 2
rs12720066
ABCB1
0.925 0.040 7 87540386 intron variant A/C snv 3.9E-02 2
rs12934241
MMP2
0.925 0.040 16 55486666 non coding transcript exon variant C/G;T snv 2
rs1326123837
SLC37A4 ; TRAPPC4
0.925 0.040 11 119025310 missense variant C/T snv 7.0E-06 2
rs1422359334
GSTK1 ; LOC105375545
0.925 0.040 7 143264131 missense variant C/A;T snv 4.0E-06 2
rs1424665740
SLC10A2
0.925 0.040 13 103066068 missense variant T/C snv 4.0E-06 7.0E-06 2
rs1482105290
DLEU2 ; TRIM13
0.925 0.040 13 50012772 missense variant A/G snv 4.0E-06 2
rs1610696
HLA-G
0.925 0.040 6 29831026 3 prime UTR variant C/G snv 0.29 2
rs17501331
ABCC1
0.925 0.040 16 15995584 intron variant A/G snv 7.7E-02 2
rs1885301
ABCC2
0.925 0.040 10 99781296 upstream gene variant A/G snv 0.58 2