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: rs1555446576
rs1555446576
1 1.000 0.120 16 2092954 missense variant C/T snv 0.800 1.000 20 1996 2009