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: rs28531779
rs28531779
1 1.000 0.040 15 32030401 intron variant G/C snv 3.2E-02 0.010 < 0.001 1 2015 2015
dbSNP: rs3087454
rs3087454
1 1.000 0.040 15 32028764 intron variant C/A;G;T snv 0.58 0.010 1.000 1 2009 2009