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: rs2227589
rs2227589
3 0.925 0.120 1 173917078 intron variant C/T snv 9.6E-02 0.030 1.000 3 2013 2019