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: rs2395185
rs2395185
17 0.724 0.360 6 32465390 intron variant G/T snv 0.29 0.810 1.000 4 2009 2012
dbSNP: rs9268877
rs9268877
5 0.827 0.200 6 32463370 intron variant A/G;T snv 0.810 1.000 3 2008 2018
dbSNP: rs9268853
rs9268853
10 0.790 0.440 6 32461866 intron variant T/C snv 0.29 0.800 1.000 1 2011 2011
dbSNP: rs9268923
rs9268923
2 1.000 0.040 6 32465058 intron variant C/T snv 0.29 0.800 1.000 1 2010 2010