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: rs2047937
rs2047937
5 0.925 0.120 16 49830880 intron variant C/T snv 0.50 0.700 1.000 2 2018 2019
dbSNP: rs34050011
rs34050011
1 16 49834602 intron variant C/A snv 0.40 0.700 1.000 1 2019 2019