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: rs3024493
rs3024493
9 0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs145922845
rs145922845
1 1.000 0.040 1 206772393 missense variant C/T snv 1.9E-03 1.8E-03 0.030 0.667 3 2000 2005
dbSNP: rs1800871
rs1800871
108 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.020 1.000 2 2009 2016
dbSNP: rs1800896
rs1800896
113 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2011 2016
dbSNP: rs2222202
rs2222202
5 0.827 0.160 1 206772036 intron variant G/A snv 0.39 0.010 1.000 1 2009 2009