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: rs16969968
rs16969968
37 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 0.100 1.000 29 2008 2018
dbSNP: rs588765
rs588765
6 0.827 0.200 15 78573083 intron variant T/A;C snv 0.010 1.000 1 2013 2013
dbSNP: rs660652
rs660652
3 1.000 0.080 15 78595490 3 prime UTR variant A/G;T snv 0.010 1.000 1 2010 2010