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: rs2032487
rs2032487
3 0.882 0.080 22 36299382 intron variant C/T snv 0.78 0.020 1.000 2 2009 2012
dbSNP: rs3752462
rs3752462
7 0.827 0.160 22 36314138 splice region variant T/C snv 0.57 0.53 0.010 1.000 1 2012 2012
dbSNP: rs4821480
rs4821480
9 0.807 0.160 22 36299201 intron variant G/T snv 0.78 0.010 1.000 1 2009 2009
dbSNP: rs4821481
rs4821481
1 1.000 0.080 22 36299896 intron variant C/T snv 0.78 0.010 1.000 1 2009 2009