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: rs777774802
rs777774802
2 1.000 0.120 4 186209194 missense variant C/T snv 2.8E-05 1.4E-05 0.010 1.000 1 2018 2018