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: rs146534657
rs146534657
1 1.000 0.120 6 137874854 missense variant A/G snv 1.4E-02 6.0E-03 0.010 1.000 1 2015 2015
dbSNP: rs719149
rs719149
1 1.000 0.120 6 137871608 intron variant G/A snv 0.19 0.010 1.000 1 2012 2012
dbSNP: rs77191406
rs77191406
12 0.790 0.280 6 137881704 3 prime UTR variant C/T snv 7.2E-04 0.010 1.000 1 2016 2016
dbSNP: rs582757
rs582757
8 0.776 0.320 6 137876687 intron variant C/T snv 0.70 0.020 1.000 2 2009 2015
dbSNP: rs2230926
rs2230926
27 0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 0.080 1.000 8 2010 2017
dbSNP: rs5029924
rs5029924
4 0.851 0.200 6 137866361 intron variant C/T snv 0.13 0.700 1.000 1 2017 2017
dbSNP: rs5029949
rs5029949
2 0.925 0.120 6 137876369 intron variant A/G snv 8.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs5029937
rs5029937
4 0.882 0.160 6 137874014 intron variant G/T snv 0.13 0.740 1.000 5 2009 2017