Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs387907021
DNAL1
0.925 0.160 14 73689432 missense variant A/G snv 3
rs876657637
DNAL1
1.000 14 73671556 frameshift variant TATCTTT/- delins 1.4E-05 2