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: rs964184
rs964184
12 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.800 1.000 6 2009 2019
dbSNP: rs12286037
rs12286037
6 1.000 0.040 11 116781491 intron variant C/T snv 0.11 0.800 1.000 1 2012 2019
dbSNP: rs2075290
rs2075290
7 0.882 0.160 11 116782580 intron variant C/G;T snv 0.800 1.000 1 2011 2019
dbSNP: rs2266788
rs2266788
7 0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 0.800 1.000 1 2011 2018
dbSNP: rs12285095
rs12285095
4 11 116787315 non coding transcript exon variant T/G snv 9.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs2072560
rs2072560
5 11 116791110 missense variant T/C snv 0.89 0.94 0.700 1.000 1 2012 2012