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: rs1045118320
rs1045118320
3 0.925 9 128332219 missense variant C/A snv 7.0E-06 0.700 1.000 13 2005 2017
dbSNP: rs758522459
rs758522459
3 0.925 9 128323147 missense variant G/C snv 4.3E-05 7.0E-05 0.700 1.000 13 2005 2017