Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10429489 0.925 0.080 9 21787522 intergenic variant G/A snv 0.26 2
rs12296850 0.925 0.080 12 100426307 downstream gene variant A/G snv 8.7E-02 2
rs17635492 1.000 0.080 6 117450114 intron variant A/T snv 2.4E-02 2
rs2018683 1.000 0.080 7 28974579 intergenic variant G/A;T snv 2
rs344924 1.000 0.080 1 67639770 intergenic variant A/G snv 0.17 2
rs7186128 1.000 0.080 16 16864058 intergenic variant G/A snv 0.70 2
rs9295740 0.827 0.120 6 27721723 intergenic variant G/A snv 0.27 2
rs11674251 1.000 0.080 2 20016748 upstream gene variant T/C snv 0.18 1
rs1209950 1.000 0.080 21 38801604 upstream gene variant C/T snv 0.30 1
rs12621220 1.000 0.080 2 112840678 non coding transcript exon variant C/T snv 0.24 1
rs1454694 0.827 0.080 4 181276794 intergenic variant T/C snv 0.20 1
rs16950650
ABCC4
1.000 0.080 13 95123178 intron variant C/T snv 4.7E-02 2
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 5
rs3114020
ABCG2
0.882 0.200 4 88162514 intron variant T/C snv 0.40 3
rs2231137
ABCG2
0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02 1
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 9
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 2
rs778561687
AKT2
0.851 0.080 19 40235953 missense variant C/A;T snv 4.0E-06; 4.0E-06 1
rs113994088
ALK
0.925 0.080 2 29222584 missense variant C/G snv 3
rs1057519698
ALK
0.827 0.120 2 29222347 missense variant A/G;T snv 2
rs113994091
ALK
0.882 0.160 2 29222407 missense variant G/A;C snv 3.2E-05 2
rs281864719
ALK
0.763 0.240 2 29220831 missense variant A/C;G;T snv 2
rs863225283
ALK
0.925 0.080 2 29213993 missense variant A/C snv 2
rs1057519781
ALK
0.807 0.160 2 29209816 missense variant C/G snv 1
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 1