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: rs13428823
rs13428823
2 2 25150429 intron variant G/A snv 0.59 0.700 1.000 1 2013 2013
dbSNP: rs34517663
rs34517663
1 2 25125723 intron variant A/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs519111
rs519111
1 2 25110866 intron variant T/C snv 0.36 0.700 1.000 1 2017 2017
dbSNP: rs6733301
rs6733301
4 0.925 0.080 2 25053415 intron variant G/A snv 0.13 0.700 1.000 1 2008 2008