Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs57749775
KRT8
0.851 0.080 12 52904822 missense variant A/G;T snv 1.7E-03; 4.0E-06 6
rs10433937
HSD17B13
0.882 0.080 4 87308948 intron variant T/A;C;G snv 4
rs10020432
AFP
0.925 0.080 4 73455883 3 prime UTR variant A/G snv 0.54 2
rs1140409
MIR3064 ; DDX5
0.925 0.080 17 64500552 missense variant A/C snv 5.4E-02 5.0E-02 2
rs12104272
SCAF1
0.925 0.080 19 49644795 intron variant G/A snv 0.44 2
rs1227756
COL13A1
0.925 0.080 10 69828748 intron variant G/A;C snv 2
rs2298839
AFP
0.925 0.080 4 73445127 splice region variant A/G;T snv 0.54 2
rs2679757
AZIN1
0.925 0.080 8 102858590 intron variant A/G snv 0.37 2
rs2710833
DDX60L ; LOC107986198
0.925 0.080 4 168488807 intron variant T/A;C snv 2
rs343064 0.925 0.080 7 35515178 upstream gene variant C/G;T snv 2
rs4646038
CASP9
0.925 0.080 1 15506705 intron variant C/T snv 7.0E-06 2
rs571462252
KRT8
0.925 0.080 12 52904720 missense variant G/A 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
rs6591182
EHBP1L1
0.925 0.080 11 65582285 missense variant T/G snv 0.47 0.45 2
rs675520
LOC102723649 ; LOC105378018
0.925 0.080 6 137672095 non coding transcript exon variant A/G;T snv 2
rs6834059
AFP
0.925 0.080 4 73435958 intron variant C/G snv 0.23 2
rs8021276 0.925 0.080 14 92110162 upstream gene variant A/G;T snv 2
rs887304
CRACR2A
0.925 0.080 12 3648382 3 prime UTR variant T/C snv 0.77 2
rs10146249
ATXN3
1.000 0.080 14 92074996 intron variant C/A snv 0.29 1
rs26311
GHRLOS ; GHRL
1.000 0.080 3 10291242 5 prime UTR variant C/G snv 0.16 1
rs3017895
FAM13A-AS1 ; FAM13A
1.000 0.080 4 88728340 3 prime UTR variant A/G snv 0.19 1
rs3730017
NOS2
1.000 0.080 17 27782076 missense variant G/A snv 3.7E-02 7.2E-02 1
rs7158733
ATXN3
1.000 0.080 14 92070879 stop gained G/A;T snv 1.2E-05; 0.27 1
rs886277
TRPM5
1.000 0.080 11 2418537 missense variant T/C snv 0.44 0.47 1