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: rs2070902
rs2070902
2 1.000 0.120 1 161217875 intron variant C/T snv 0.31 0.700 1.000 1 2018 2018