Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs140451304
CFAP410
0.882 0.120 21 44333188 missense variant C/G;T snv 3.1E-04; 8.2E-06 3
rs748531024
CFAP410
1.000 0.080 21 44339161 frameshift variant -/TGCACGCTGTGCAGCT ins 4.4E-05; 2.2E-05 7.7E-05 2