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: rs6496932
rs6496932
1 15 85282336 intron variant C/A snv 0.29 0.800 1.000 1 2013 2013
dbSNP: rs10163187
rs10163187
1 15 85327287 intron variant C/T snv 0.29 0.700 1.000 1 2013 2013