Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6759676 2 113078771 downstream gene variant C/T snv 0.56 1
rs12711751 2 113080188 downstream gene variant T/G snv 0.61 2
rs13409360 2 113080525 downstream gene variant G/A snv 0.38 2
rs13409371 2 113080568 downstream gene variant G/A;C;T snv 1
rs6734238 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 8
rs6781222 3 115407022 intron variant G/A snv 0.41 1
rs3822857
FRK
6 115992768 intron variant G/A;C snv 3
rs12202641
FRK
6 115993471 intron variant C/A;T snv 1
rs2064009
LINC00536
8 115995625 intron variant C/G;T snv 1
rs6987444
LINC00536
8 116064090 intron variant G/A snv 0.68 1
rs1396485
COMMD10
5 116176655 intron variant G/A snv 0.32 1
rs6901250
GPRC6A
6 116792862 synonymous variant G/A snv 0.33 0.29 1
rs1736060
FDFT1
8 11807229 intron variant C/G;T snv 0.54 1
rs1616534
FDFT1
8 11808942 intron variant C/G;T snv 9.8E-06; 0.58 1
rs10435719 8 11919395 downstream gene variant C/T snv 0.48 2
rs2686555
CABP1
12 120657369 intron variant A/G snv 0.52 2
rs4871137 8 120856311 intergenic variant G/T snv 0.55 2
rs2649999
HNF1A-AS1
12 120942741 intron variant T/C snv 0.70 1
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 10
rs7305618
HNF1A-AS1
0.925 0.160 12 120965129 intron variant C/T snv 0.28 3
rs7953249
HNF1A-AS1
0.882 0.160 12 120965921 splice region variant G/A snv 0.59 4
rs1920792
HNF1A-AS1
1.000 0.080 12 120966781 intron variant T/C snv 0.43 2
rs2251468
HNF1A-AS1
12 120967323 intron variant C/A;G;T snv 2
rs10774579
HNF1A-AS1
12 120967407 intron variant T/C snv 0.43 1
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21