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: rs6545814
rs6545814
3 2 24908447 intron variant A/G snv 0.53 0.700 1.000 2 2012 2014
dbSNP: rs11676272
rs11676272
5 1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57 0.700 1.000 1 2012 2012
dbSNP: rs7586879
rs7586879
3 2 24894108 intron variant C/T snv 0.47 0.700 1.000 1 2013 2013