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: rs11247361
rs11247361
1 1.000 0.080 15 98664163 intron variant C/G;T snv 0.29 0.010 1.000 1 2016 2016
dbSNP: rs2249350
rs2249350
3 1.000 0.080 21 26950187 intron variant C/A snv 9.7E-02 0.010 1.000 1 2016 2016