Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs26311
GHRLOS ; GHRL
1.000 0.080 3 10291242 5 prime UTR variant C/G snv 0.16 1
rs3730017
NOS2
1.000 0.080 17 27782076 missense variant G/A snv 3.7E-02 7.2E-02 1
rs886277
TRPM5
1.000 0.080 11 2418537 missense variant T/C snv 0.44 0.47 1
rs343064 0.925 0.080 7 35515178 upstream gene variant C/G;T snv 2
rs643608 0.925 0.080 21 43348682 intergenic variant C/T snv 0.69 2
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
rs9380516 0.925 0.120 6 35534425 TF binding site variant T/C snv 0.85 2
rs10020432
AFP
0.925 0.080 4 73455883 3 prime UTR variant A/G snv 0.54 2
rs2298839
AFP
0.925 0.080 4 73445127 splice region variant A/G;T snv 0.54 2
rs6834059
AFP
0.925 0.080 4 73435958 intron variant C/G snv 0.23 2
rs2679757
AZIN1
0.925 0.080 8 102858590 intron variant A/G snv 0.37 2
rs4646038
CASP9
0.925 0.080 1 15506705 intron variant C/T snv 7.0E-06 2
rs1227756
COL13A1
0.925 0.080 10 69828748 intron variant G/A;C snv 2
rs887304
CRACR2A
0.925 0.080 12 3648382 3 prime UTR variant T/C snv 0.77 2
rs2710833
DDX60L ; LOC107986198
0.925 0.080 4 168488807 intron variant T/A;C snv 2
rs6591182
EHBP1L1
0.925 0.080 11 65582285 missense variant T/G snv 0.47 0.45 2
rs1201810520
EIF2AK3
0.925 0.160 2 88590497 missense variant C/T snv 2
rs1545224
FABP1
0.925 0.120 2 88124297 3 prime UTR variant A/G snv 0.18 2
rs2629751
GLT8D2
0.925 0.120 12 104028030 intron variant A/G snv 0.36 2
rs747432300
GPT ; LOC101928953
0.925 0.120 8 144504357 missense variant C/A;T snv 8.1E-06; 1.2E-04 2
rs642588
IGF2R
0.925 0.120 6 159990235 intron variant A/G snv 0.83 2