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: rs9272219
rs9272219
4 0.925 0.160 6 32634492 intron variant G/T snv 0.29 0.710 1.000 2 2011 2014
dbSNP: rs2187668
rs2187668
10 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 0.700 1.000 3 2007 2011
dbSNP: rs2040406
rs2040406
3 0.882 0.240 6 32635230 intron variant A/G snv 0.23 0.700 1.000 1 2011 2011
dbSNP: rs9272346
rs9272346
6 0.790 0.320 6 32636595 intron variant G/A snv 0.54 0.700 1.000 1 2011 2011
dbSNP: rs9272535
rs9272535
5 0.827 0.280 6 32638979 synonymous variant G/A snv 3.0E-05 1.8E-03 0.700 1.000 1 2011 2011
dbSNP: rs9272723
rs9272723
2 0.925 0.200 6 32641650 intron variant T/C snv 0.700 1.000 1 2011 2011
dbSNP: rs9272853
rs9272853
1 1.000 0.120 6 32642928 3 prime UTR variant G/A;C;T snv 1.0E-02 0.700 1.000 1 2011 2011