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: rs266085
rs266085
5 0.851 0.200 10 44378805 intron variant C/T snv 0.32 0.020 1.000 2 2009 2015
dbSNP: rs17885289
rs17885289
3 0.882 0.080 10 44386212 non coding transcript exon variant C/T snv 0.26 0.010 1.000 1 2009 2009
dbSNP: rs266093
rs266093
3 0.882 0.080 10 44370760 3 prime UTR variant C/G;T snv 0.010 1.000 1 2009 2009