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: rs2073716
rs2073716
1 1.000 0.200 6 31155220 intron variant C/G snv 6.8E-02 0.700 1.000 1 2012 2012