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: rs1894116
rs1894116
1 1.000 0.120 11 102199908 intron variant A/G snv 8.2E-02 0.800 1.000 1 2012 2012
dbSNP: rs11225154
rs11225154
1 1.000 0.120 11 102172509 intron variant G/A;C snv 0.700 1.000 2 2015 2018