Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs747432300
GPT ; LOC101928953
0.925 0.120 8 144504357 missense variant C/A;T snv 8.1E-06; 1.2E-04 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
rs9380516 0.925 0.120 6 35534425 TF binding site variant T/C snv 0.85 2
rs2289030
MIR492 ; KRT19P2
0.882 0.120 12 94834510 non coding transcript exon variant G/C snv 9.7E-02 6.3E-02 6
rs10433937
HSD17B13
0.882 0.080 4 87308948 intron variant T/A;C;G snv 4
rs2217332
HERPUD1
0.882 0.160 16 56935236 missense variant G/A snv 0.15 0.14 4
rs7254880
ZNF699
0.882 0.160 19 9298599 intron variant C/G snv 0.16 4
rs1059122
FAM13A-AS1 ; FAM13A
0.882 0.160 4 88726273 3 prime UTR variant T/A snv 0.46 3
rs10945859
PRKN
0.882 0.120 6 162721570 intron variant T/C snv 0.17 3
rs1358379
LINC00472 ; MIR30A
0.882 0.160 6 71403739 intron variant T/C snv 6.2E-02 3
rs137853590
PHKG2
0.882 0.160 16 30751140 stop gained C/T snv 4.0E-06 3
rs1431315635
HFE ; LOC108783645
0.882 0.120 6 26092928 missense variant C/T snv 4.0E-06 3
rs1485766
VEGFC ; LOC105377555
0.882 0.120 4 176689730 intron variant T/A;G snv 3
rs26907
RASGRF2
0.882 0.240 5 81069496 intron variant G/A;T snv 3
rs2843403
MMEL1
0.882 0.200 1 2597658 intron variant T/C snv 0.54 3
rs3106796
COL3A1 ; LOC105373791
0.882 0.160 2 188985047 non coding transcript exon variant A/G snv 0.35 3
rs376373278
MPO
0.882 0.120 17 58279015 missense variant G/A;C snv 4.2E-06 3
rs3820998
TANK ; LOC105373719
0.882 0.120 2 161138615 intron variant C/A;T snv 3
rs3844942 0.882 0.120 4 189571800 intergenic variant T/C snv 3
rs3859501
MIR371B ; MIR373 ; MIR372 ; MIR371A
0.882 0.120 19 53788157 non coding transcript exon variant A/C snv 0.43 3
rs56073403
AGT
0.882 0.160 1 230710009 missense variant T/C snv 7.2E-04 6.8E-04 3
rs7536540
MIR101-1 ; MIR3671 ; JAK1
0.882 0.160 1 65058899 intron variant C/G;T snv 0.65 3