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: rs8032158
rs8032158
1 1.000 0.080 15 55902679 intron variant T/A;C snv 0.810 1.000 2 2010 2013
dbSNP: rs2271289
rs2271289
1 1.000 0.080 15 55924595 non coding transcript exon variant C/T snv 0.33 0.010 1.000 1 2013 2013