Source: ALL
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: rs2032487
rs2032487
MYH9
3 0.882 0.080 22 36299382 intron variant C/T snv 0.78 0.010 1.000 1 2012 2012