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: rs141970897
rs141970897
8 0.925 0.200 9 129104269 missense variant T/C snv 1.1E-03 7.8E-04 0.700 1.000 1 2020 2020
dbSNP: rs762425351
rs762425351
8 0.925 0.200 9 129095573 missense variant C/T snv 1.2E-04 7.7E-05 0.700 1.000 1 2020 2020