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: rs3801266
rs3801266
3 0.925 0.080 7 106283804 intron variant T/C snv 0.26 0.020 1.000 2 2012 2015
dbSNP: rs4730153
rs4730153
3 0.882 0.120 7 106263704 intron variant A/G snv 0.49 0.020 1.000 2 2008 2016
dbSNP: rs1319501
rs1319501
4 0.882 0.120 7 106285307 intron variant C/A;T snv 0.76 0.010 1.000 1 2015 2015