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: rs11193085
rs11193085
3 10 106873848 intron variant G/A snv 8.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs11813704
rs11813704
2 10 107102114 intron variant G/T snv 3.1E-02 0.700 1.000 1 2012 2012