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: rs2071348
rs2071348
1 1.000 0.080 11 5242916 intron variant T/G snv 0.25 0.700 1.000 1 2010 2010