Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs57137919
ABCG1 ; LOC105372814
0.776 0.160 21 42218908 intron variant G/A snv 0.14 9
rs1294780786
ABCG1
0.925 0.080 21 42282350 missense variant G/A;T snv 4.0E-06; 4.0E-06 2
rs1445295054
ABCG1
0.925 0.080 21 42282356 missense variant G/A;T snv 4.0E-06 2
rs1378577
ABCG1
1.000 0.080 21 42199555 upstream gene variant T/G snv 0.33 2
rs750249283
ABCG1
0.925 0.080 21 42296256 missense variant C/G;T snv 4.0E-06; 8.0E-06 2
rs492338
ABCG1
21 42281867 intron variant A/G snv 0.52 2
rs225396
ABCG1
0.925 0.040 21 42267244 intron variant C/T snv 0.45 2
rs182694
ABCG1
1.000 0.040 21 42278705 intron variant A/G;T snv 1
rs2234714
ABCG1 ; LOC105372814
1.000 0.040 21 42218507 intron variant G/A snv 0.33 1