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: rs17531088
rs17531088
1 1.000 0.120 3 175175985 intron variant C/T snv 0.34 0.800 1.000 1 2009 2009