Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4646437
CYP3A4
0.827 0.200 7 99767460 intron variant G/A snv 0.30 8
rs2233682
PIN1
0.827 0.240 19 9838476 synonymous variant G/A snv 3.7E-02 6.3E-02 5
rs705382
PON1
0.827 0.200 7 95325909 upstream gene variant C/G snv 0.53 5
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs2289030
MIR492 ; KRT19P2
0.882 0.120 12 94834510 non coding transcript exon variant G/C snv 9.7E-02 6.3E-02 6
rs767864210
PDLIM5
0.882 0.120 4 94657500 missense variant G/A;T snv 8.0E-05 2.1E-05 3
rs17580
SERPINA1
0.776 0.160 14 94380925 missense variant T/A snv 2.3E-02 2.9E-02 14
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs7254880
ZNF699
0.882 0.160 19 9298599 intron variant C/G snv 0.16 4
rs6487679 0.925 0.080 12 9218736 intergenic variant C/T snv 0.80 2
rs8021276 0.925 0.080 14 92110162 upstream gene variant A/G;T snv 2
rs10146249
ATXN3
1.000 0.080 14 92074996 intron variant C/A snv 0.29 1
rs7158733
ATXN3
1.000 0.080 14 92070879 stop gained G/A;T snv 1.2E-05; 0.27 1
rs3017895
FAM13A-AS1 ; FAM13A
1.000 0.080 4 88728340 3 prime UTR variant A/G snv 0.19 1
rs1059122
FAM13A-AS1 ; FAM13A
0.882 0.160 4 88726273 3 prime UTR variant T/A snv 0.46 3
rs1201810520
EIF2AK3
0.925 0.160 2 88590497 missense variant C/T snv 2
rs2241883
FABP1
0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs1545224
FABP1
0.925 0.120 2 88124297 3 prime UTR variant A/G snv 0.18 2
rs72613567
HSD17B13
0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs10433937
HSD17B13
0.882 0.080 4 87308948 intron variant T/A;C;G snv 4
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs26907
RASGRF2
0.882 0.240 5 81069496 intron variant G/A;T snv 3
rs28934571
TP53
0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs4074
CXCL1
0.827 0.200 4 73870427 intron variant A/G snv 0.46 6
rs10020432
AFP
0.925 0.080 4 73455883 3 prime UTR variant A/G snv 0.54 2