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: rs77490164
rs77490164
2 0.925 0.040 6 124238586 intron variant C/T snv 4.4E-02 0.700 1.000 1 2013 2013