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: rs376289593
rs376289593
1 1.000 0.080 2 112836202 missense variant C/T snv 1.2E-04 4.9E-05 0.010 1.000 1 2019 2019