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: rs2071374
rs2071374
1 1.000 0.120 2 112779775 intron variant T/G snv 0.27 0.010 1.000 1 2008 2008