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: rs117633859
rs117633859
1 1.000 0.120 1 67162145 intron variant A/G snv 2.6E-02 0.710 1.000 1 2014 2014
dbSNP: rs3021304
rs3021304
1 1.000 0.120 6 32607881 intergenic variant G/C snv 0.51 0.710 1.000 1 2014 2014
dbSNP: rs442309
rs442309
1 1.000 0.120 10 62730735 intron variant C/T snv 0.51 0.710 1.000 1 2014 2014
dbSNP: rs114800139
rs114800139
1 1.000 0.120 6 32460938 intron variant G/A snv 0.700 1.000 1 2014 2014