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: rs9282858
rs9282858
16 0.716 0.320 2 31580756 missense variant C/T snv 1.8E-02 2.1E-02 0.710 1.000 2 2007 2017
dbSNP: rs191212334
rs191212334
1 1.000 0.080 2 31628285 intergenic variant C/G;T snv 1.3E-04 0.700 1.000 1 2017 2017