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: rs121908363
rs121908363
4 0.925 0.160 7 107710126 missense variant C/T snv 5.2E-05 2.8E-05 0.800 1.000 17 1998 2017