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: rs9632884
rs9632884
6 0.851 0.160 9 22072302 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs1333049
rs1333049
60 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.020 1.000 2 2008 2016
dbSNP: rs10757274
rs10757274
22 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.010 1.000 1 2009 2009
dbSNP: rs10757278
rs10757278
44 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.010 1.000 1 2016 2016
dbSNP: rs2383206
rs2383206
17 0.742 0.320 9 22115027 intron variant A/G snv 0.49 0.010 1.000 1 2009 2009