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: rs2075686
rs2075686
13 0.742 0.240 5 83076927 intron variant C/T snv 1.7E-02 0.010 1.000 1 2010 2010
dbSNP: rs28360071
rs28360071
18 0.708 0.240 5 83142293 intron variant GATGAGGAAACTAACTCTCAGTGGTGTTTA/- delins 0.48 0.010 1.000 1 2010 2010
dbSNP: rs28360317
rs28360317
15 0.716 0.280 5 83323739 intron variant -/CCT delins 0.24 0.010 1.000 1 2010 2010
dbSNP: rs3734091
rs3734091
19 0.689 0.280 5 83204915 missense variant G/T snv 2.3E-02 1.4E-02 0.010 1.000 1 2010 2010
dbSNP: rs7727691
rs7727691
9 0.763 0.200 5 83075876 intron variant C/T snv 0.32 0.010 1.000 1 2010 2010