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: rs3129859
rs3129859
5 0.827 0.320 6 32433162 intergenic variant G/C;T snv 0.710 1.000 1 2018 2018
dbSNP: rs2296651
rs2296651
13 0.732 0.240 14 69778476 missense variant G/A snv 6.3E-03 2.5E-03 0.010 1.000 1 2015 2015
dbSNP: rs3775291
rs3775291
51 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 0.010 1.000 1 2013 2013
dbSNP: rs7298346
rs7298346
1 1.000 0.040 12 63154939 upstream gene variant T/A;G snv 0.010 1.000 1 2017 2017
dbSNP: rs7308855
rs7308855
3 0.925 0.080 12 63154276 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2017 2017