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: rs2169876
rs2169876
1 15 85542545 intron variant T/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs258415
rs258415
1 12 27864589 intergenic variant A/C snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs4458717
rs4458717
1 6 132587740 downstream gene variant T/A;C snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs7102702
rs7102702
1 11 49379573 non coding transcript exon variant T/A;G snv 0.700 1.000 1 2011 2011