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: rs375818497
rs375818497
1 1.000 0.040 16 29813554 missense variant C/T snv 0.010 1.000 1 2019 2019