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: rs25487
rs25487
205 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.100 0.583 12 2004 2016
dbSNP: rs1799782
rs1799782
151 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.080 0.750 8 2008 2016
dbSNP: rs25489
rs25489
78 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.080 0.875 8 2007 2017
dbSNP: rs2854509
rs2854509
6 0.807 0.160 19 43570445 intron variant T/G snv 0.80 0.010 1.000 1 2015 2015
dbSNP: rs3213255
rs3213255
3 0.882 0.120 19 43573355 intron variant G/A snv 0.60 0.010 1.000 1 2015 2015
dbSNP: rs3213356
rs3213356
3 0.882 0.120 19 43554087 intron variant C/T snv 0.60 0.010 1.000 1 2016 2016