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: rs2070600
rs2070600
82 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.070 0.714 7 2001 2016
dbSNP: rs184003
rs184003
15 0.724 0.400 6 32182519 intron variant C/A snv 0.12 0.12 0.010 1.000 1 2019 2019