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: rs10897518
rs10897518
3 0.925 0.120 11 64593233 intron variant C/T snv 0.51 0.800 1.000 1 2009 2015
dbSNP: rs505802
rs505802
3 0.882 0.160 11 64589600 upstream gene variant T/C snv 0.45 0.800 1.000 1 2009 2019