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: rs4942486
rs4942486
2 13 32379251 intron variant T/C snv 0.52 0.700 1.000 1 2013 2013
dbSNP: rs9534275
rs9534275
7 0.851 0.080 13 32366208 intron variant C/A snv 0.52 0.700 1.000 1 2012 2012