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: rs17487792
rs17487792
3 0.882 0.080 2 214778776 intron variant C/T snv 0.16 0.810 1.000 3 2009 2019