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: rs504915
rs504915
3 0.925 0.120 11 64696613 intron variant T/A;C snv 0.800 1.000 2 2012 2018
dbSNP: rs57633992
rs57633992
1 11 64657495 intron variant C/A;T snv 0.700 1.000 2 2018 2019
dbSNP: rs478607
rs478607
3 0.925 0.120 11 64710591 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs490192
rs490192
3 0.925 0.120 11 64703897 intron variant G/A snv 0.33 0.700 1.000 1 2009 2009
dbSNP: rs506338
rs506338
4 0.925 0.120 11 64673448 intron variant T/C snv 0.52 0.700 1.000 1 2010 2010
dbSNP: rs544838
rs544838
3 0.925 0.120 11 64661587 intron variant T/C snv 0.52 0.700 1.000 1 2009 2009
dbSNP: rs7117423
rs7117423
3 0.925 0.120 11 64657648 intron variant G/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs7932437
rs7932437
3 0.925 0.120 11 64606032 downstream gene variant T/C snv 0.52 0.700 1.000 1 2009 2009