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: rs2253612
rs2253612
3 1.000 0.080 2 200703710 intron variant C/T snv 0.79 0.700 1.000 1 2015 2015