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: rs6511720
rs6511720
15 0.769 0.107 19 11091630 intron variant G/T snp 0.11 0.710 1.000 3 2011 2014
dbSNP: rs2228671
rs2228671
10 0.801 0.143 19 11100236 stop gained C/A,G,T snp 1.6E-05; 8.9E-02 8.6E-02 0.710 1.000 2 2011 2011
dbSNP: rs688
rs688
7 0.821 0.107 19 11116926 synonymous variant C/T snp 0.39 0.33 0.010 1.000 1 2011 2011