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: rs7020673
rs7020673
4 0.882 0.200 9 4291747 intron variant C/A;G snv 0.810 0.500 2 2009 2017
dbSNP: rs10758593
rs10758593
8 0.827 0.240 9 4292083 intron variant G/A snv 0.45 0.710 0.500 2 2011 2017
dbSNP: rs6476839
rs6476839
3 0.925 0.120 9 4290823 intron variant A/C;T snv 0.700 1.000 1 2015 2015
dbSNP: rs140101069
rs140101069
2 1.000 0.120 9 3828342 missense variant G/A snv 3.2E-04 8.4E-05 0.010 1.000 1 2013 2013