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: rs538557
rs538557
1 1.000 0.080 6 106236001 intron variant T/C snv 4.3E-02 0.700 1.000 1 2009 2009