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: rs2228145
rs2228145
57 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.700 1.000 2 2009 2013
dbSNP: rs4129267
rs4129267
13 0.807 0.200 1 154453788 intron variant C/G;T snv 0.700 1.000 2 2011 2013
dbSNP: rs4537545
rs4537545
11 0.790 0.160 1 154446403 intron variant C/T snv 0.48 0.700 1.000 1 2011 2011
dbSNP: rs7518199
rs7518199
4 1 154434943 intron variant A/C;T snv 0.39; 4.2E-06 0.700 1.000 1 2011 2011
dbSNP: rs7529229
rs7529229
8 0.851 0.120 1 154448302 intron variant T/C snv 0.48 0.700 1.000 1 2011 2011