Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1034207 6 127016554 intron variant C/A;G;T snv 0.94 1
rs11154370 6 126846446 intron variant A/G;T snv 1
rs1443512 12 53948900 downstream gene variant A/C;T snv 1
rs17568628 5 76751114 intergenic variant T/C;G snv 1
rs2119690 8 20002028 intergenic variant G/A;C snv 1
rs2145272 20 6645571 intergenic variant G/A;T snv 1
rs4580892 6 127088737 intron variant C/T snv 0.32 1
rs4846567 1 219577375 regulatory region variant G/T snv 0.23 1
rs645040 3 136207780 upstream gene variant G/T snv 0.77 1
rs757608 17 61419916 regulatory region variant A/G;T snv 1
rs7797307 7 69221140 intron variant G/C snv 7.6E-02 1
rs9750952 1.000 0.080 2 238827723 intergenic variant C/T snv 0.19 1
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 1
rs1254319
C14orf39
1.000 14 60437039 missense variant G/A snv 0.35 0.36 1
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 1
rs505102
CFH
1 196650372 upstream gene variant T/C snv 0.40 1
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 1
rs9515201
COL4A2
0.925 0.080 13 110388451 intron variant A/C snv 0.63 1
rs6861681
CPEB4
5 173935455 intron variant G/A snv 0.22 1
rs6942652
CPED1
7 121249218 intron variant G/C;T snv 1
rs11724804
DGKQ
0.882 0.160 4 971991 intron variant G/A snv 0.43 1
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 1
rs605203
EHMT2-AS1 ; LOC107986588 ; CYP21A2 ; SLC44A4
1.000 0.120 6 31879235 intron variant C/A snv 0.77 1
rs9647379
FNDC3B
3 172067378 intron variant G/C snv 0.32 1
rs9302652
FTO
1.000 0.080 16 53832063 intron variant C/T snv 0.74 1