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: rs1805097
rs1805097
21 0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 0.100 1.000 12 2000 2017
dbSNP: rs137852740
rs137852740
1 1.000 0.080 13 109784115 missense variant G/A;C snv 2.2E-05; 9.3E-05 0.010 1.000 1 2003 2003