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: rs174577
rs174577
13 1.000 0.080 11 61837342 intron variant C/A snv 0.38 0.700 1.000 1 2016 2016