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: rs10007052
rs10007052
1 1.000 0.040 4 141084419 intron variant C/A snv 0.31 0.710 1.000 1 2012 2015