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: rs786204014
rs786204014
1 1.000 1 11796399 missense variant C/T snv 0.800 1.000 7 1995 2015