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: rs9979383
rs9979383
5 0.925 0.200 21 35343463 intron variant C/G;T snv 0.800 1.000 3 2012 2016
dbSNP: rs8133843
rs8133843
1 1.000 0.120 21 35365944 intron variant G/A snv 0.65 0.800 1.000 2 2014 2019
dbSNP: rs2051179
rs2051179
1 1.000 0.120 21 34954256 intron variant A/T snv 0.57 0.010 1.000 1 2012 2012
dbSNP: rs2268277
rs2268277
1 1.000 0.120 21 34809752 intron variant G/A;C snv 0.010 1.000 1 2008 2008