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: rs10043986
rs10043986
2 0.925 0.040 5 79799594 missense variant C/T snv 8.7E-02 8.2E-02 0.010 1.000 1 2019 2019