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: rs2242663
rs2242663
1 1.000 0.040 11 66567837 intron variant T/C snv 0.23 0.800 1.000 1 2009 2009