Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11887534
ABCG5 ; ABCG8
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 25
rs4148217
ABCG8
0.790 0.280 2 43872294 missense variant C/A;T snv 0.21; 1.2E-05 8
rs6544718
ABCG8
0.882 0.120 2 43877786 missense variant T/A;C;G snv 0.84; 4.0E-06 4
rs4148211
ABCG8 ; LOC102725159
0.882 0.080 2 43844604 missense variant A/G snv 0.43 0.35 3
rs749661564
ABCG8
0.925 0.040 2 43852775 missense variant C/T snv 4.0E-06 2
rs4245791
ABCG8
0.882 0.080 2 43847292 non coding transcript exon variant C/A;T snv 2
rs1205128669
ABCG8
0.925 0.040 2 43877848 missense variant G/A;C snv 4.0E-06 2
rs755130225
ABCG8
0.925 0.040 2 43877845 missense variant G/A snv 8.0E-06 2
rs147194762
ABCG8
0.925 0.040 2 43873860 missense variant A/C;G snv 8.0E-06; 3.8E-04 2
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 2
rs6756629
ABCG5 ; ABCG8
0.925 0.080 2 43837951 missense variant G/A;T snv 6.7E-02 1
rs137852988
ABCG8
1.000 0.120 2 43875377 missense variant G/A snv 6.4E-05 2.2E-04 1
rs4953023
ABCG8
0.925 0.040 2 43846861 non coding transcript exon variant G/A snv 6.9E-02 1
rs1209143268
ABCG8
1.000 0.040 2 43877840 missense variant T/G snv 8.0E-06 1
rs137854891
ABCG8 ; LOC102725159
1.000 0.120 2 43846309 stop gained C/G snv 1.6E-05 1
rs41360247
ABCG8 ; LOC102725159
0.882 0.080 2 43846517 non coding transcript exon variant T/C snv 7.9E-02 1