Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10774671
OAS1
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs1131454
OAS1
0.882 0.040 12 112911065 missense variant G/A;C snv 0.57 3
rs2240190
OAS1
1.000 0.040 12 112908322 intron variant C/A snv 4.9E-02 1