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: rs2228638
rs2228638
NRP1
3 1.000 0.080 10 33186354 missense variant C/T snv 0.12 9.4E-02 0.820 1.000 3 2013 2018