Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2471738
rs2471738
MAPT ; STH
4 0.882 0.160 17 45998697 intron variant C/T snv 0.18 0.030 1.000 3 2009 2017