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: rs6911490
rs6911490
1 1.000 0.040 6 106074152 intron variant T/C snv 0.86 0.800 1.000 1 2011 2011
dbSNP: rs28701841
rs28701841
5 0.827 0.120 6 106082455 intron variant G/A snv 7.6E-02 0.700 1.000 1 2016 2016
dbSNP: rs4946717
rs4946717
6 0.827 0.120 6 106026874 intron variant C/A;G;T snv 0.700 1.000 1 2016 2016