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: rs12193446
rs12193446
3 0.925 0.040 6 129498893 intron variant A/G snv 6.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs1889891
rs1889891
1 1.000 0.040 6 129492201 non coding transcript exon variant C/T snv 0.37 0.010 1.000 1 2016 2016
dbSNP: rs9321170
rs9321170
1 1.000 0.040 6 129501692 intron variant G/A;C snv 0.010 1.000 1 2016 2016