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: rs270636
rs270636
2 1.000 0.080 5 5074712 intron variant C/A snv 0.39 0.700 1.000 1 2018 2018