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: rs2968857
rs2968857
2 1.000 0.080 7 150965242 intron variant C/T snv 0.70 0.010 1.000 1 2009 2009