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: rs10490924
rs10490924
16 0.716 0.240 10 122454932 missense variant G/T snv 0.26 0.23 0.050 1.000 5 2009 2018
dbSNP: rs10664316
rs10664316
1 1.000 10 122456869 intron variant -/A;AC ins 7.7E-05 0.010 1.000 1 2009 2009