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: rs2070600
rs2070600
82 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.710 1.000 3 2007 2011
dbSNP: rs1800625
rs1800625
39 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 0.700 1.000 1 2011 2011
dbSNP: rs3131300
rs3131300
1 1.000 0.120 6 32184157 non coding transcript exon variant A/G snv 0.14 0.14 0.700 1.000 1 2011 2011
dbSNP: rs3134940
rs3134940
2 0.925 0.200 6 32182039 intron variant T/C snv 0.13 0.14 0.700 1.000 1 2011 2011
dbSNP: rs8365
rs8365
1 1.000 0.120 6 32180626 3 prime UTR variant G/C snv 0.14 0.700 1.000 1 2011 2011