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: rs2040406
rs2040406
3 0.882 0.240 6 32635230 intron variant A/G snv 0.23 0.800 1.000 1 2010 2010
dbSNP: rs3104373
rs3104373
2 0.925 0.120 6 32632598 intron variant T/C snv 0.85 0.700 1.000 1 2016 2016
dbSNP: rs9272346
rs9272346
8 0.790 0.320 6 32636595 intron variant G/A snv 0.54 0.700 1.000 1 2007 2007