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: rs1135889
rs1135889
1 1.000 0.040 17 75930040 missense variant C/A snv 0.19 0.21 0.700 1.000 1 2018 2018