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: rs2004375
rs2004375
1 1.000 0.080 8 128990484 intron variant C/T snv 0.16 0.700 1.000 2 2009 2012