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: rs3817198
rs3817198
8 0.790 0.280 11 1887776 intron variant T/C snv 0.26 0.800 0.938 16 2007 2017
dbSNP: rs1973765
rs1973765
3 1.000 0.080 11 1877434 intron variant T/C snv 0.37 0.700 1.000 1 2017 2017
dbSNP: rs4980383
rs4980383
1 1.000 0.080 11 1880867 non coding transcript exon variant C/T snv 0.37 0.700 1.000 1 2016 2016
dbSNP: rs569550
rs569550
6 0.925 0.080 11 1865838 intron variant T/G snv 0.35 0.010 1.000 1 2015 2015
dbSNP: rs592373
rs592373
5 0.925 0.080 11 1869760 intron variant G/A;T snv 0.63; 6.8E-06 0.010 1.000 1 2015 2015