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: rs2331291
rs2331291
1 1.000 0.080 22 26662857 intron variant C/T snv 0.11 0.710 1.000 1 2006 2006