Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs63750869
MAPT
0.827 0.160 17 46018707 missense variant G/A snv 2.4E-05 5.6E-05 6
rs10814083
KIF24
0.882 0.160 9 34256349 synonymous variant C/T snv 0.40 0.34 3
rs201148958
IFT74
1.000 0.120 9 26978180 missense variant G/A snv 1.8E-04 6.3E-05 1