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: rs7750641
rs7750641
6 0.807 0.360 6 31161533 missense variant C/T snv 7.0E-02 7.6E-02 0.700 1.000 1 2012 2012