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: rs1922585
rs1922585
1 16 7236820 intron variant A/G snv 0.78 0.700 1.000 1 2013 2013
dbSNP: rs7185684
rs7185684
1 16 7231940 intron variant G/C snv 0.77 0.700 1.000 1 2013 2013
dbSNP: rs7204582
rs7204582
1 16 6691578 intron variant A/G snv 0.16 0.700 1.000 1 2012 2012
dbSNP: rs9924951
rs9924951
2 16 7454852 intron variant G/A snv 0.39 0.700 1.000 1 2008 2008