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: rs212528
rs212528
3 0.925 0.040 1 21259168 intron variant T/C snv 0.12 0.020 1.000 2 2007 2014
dbSNP: rs213045
rs213045
5 0.851 0.120 1 21290752 intron variant G/T snv 0.44 0.010 1.000 1 2014 2014