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: rs6234
rs6234
8 0.851 0.160 5 96393270 missense variant G/C snv 0.27 0.24 0.700 1.000 1 2015 2015
dbSNP: rs6235
rs6235
8 0.925 0.120 5 96393194 missense variant C/G snv 0.26 0.23 0.700 1.000 1 2013 2013