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: rs2071543
rs2071543
1 0.925 0.200 6 32843852 missense variant G/T snv 0.14 0.13 0.700 1.000 2 2007 2009
dbSNP: rs9357155
rs9357155
2 1.000 0.120 6 32842071 non coding transcript exon variant G/A;C snv 0.700 1.000 2 2007 2009
dbSNP: rs2071540
rs2071540
2 0.925 0.200 6 32845139 non coding transcript exon variant T/C snv 0.61 0.700 1.000 1 2009 2009
dbSNP: rs6924102
rs6924102
2 0.925 0.200 6 32843606 non coding transcript exon variant A/G snv 0.40 0.700 1.000 1 2009 2009