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: rs6589602
rs6589602
1 11 117166349 intron variant T/C snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs7122944
rs7122944
1 11 117163903 non coding transcript exon variant G/A;T snv 4.0E-06; 0.81 0.87 0.700 1.000 1 2012 2012
dbSNP: rs7940310
rs7940310
2 11 117153765 intron variant T/A;C snv 0.700 1.000 1 2012 2012