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: rs13048019
rs13048019
1 1.000 0.080 21 31545981 intron variant C/T snv 0.14 0.810 1.000 2 2010 2014