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: rs2165241
rs2165241
15 0.716 0.360 15 73929861 intron variant T/C snv 0.60 0.010 1.000 1 2017 2017
dbSNP: rs3825942
rs3825942
15 0.716 0.320 15 73927241 missense variant G/A;C;T snv 0.18; 4.5E-06 0.010 1.000 1 2011 2011