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: rs6478108
rs6478108
10 0.763 0.200 9 114796423 intron variant C/T snv 0.73 0.810 1.000 3 2009 2016
dbSNP: rs10114470
rs10114470
4 0.882 0.080 9 114785492 3 prime UTR variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs4366152
rs4366152
1 1.000 0.040 9 114802595 intron variant T/C snv 0.75 0.700 1.000 1 2015 2015
dbSNP: rs4979462
rs4979462
7 0.790 0.240 9 114804733 intron variant C/T snv 0.13 0.010 1.000 1 2016 2016
dbSNP: rs6478109
rs6478109
12 0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 0.010 1.000 1 2016 2016