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: rs2107732
rs2107732
1 1.000 0.040 7 45038379 missense variant G/A snv 6.3E-02 6.1E-02 0.700 1.000 1 2018 2018