Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1553621496
UNC80
0.677 0.440 2 209976305 splice donor variant T/G snv 53
rs886039469
KCNMA1-AS1 ; KCNMA1
0.701 0.560 10 76891709 missense variant T/C snv 34
rs1060499548
ABL1
0.724 0.440 9 130872961 missense variant G/A snv 27
rs1564421528
WAC
0.882 0.080 10 28614666 stop gained C/T snv 16