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: rs12411988
rs12411988
1 1.000 0.120 10 63555637 intron variant G/C snv 0.12 0.800 1.000 1 2012 2012
dbSNP: rs16918575
rs16918575
1 1.000 0.120 10 63541565 intron variant A/G snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs4746201
rs4746201
1 1.000 0.120 10 63562621 intron variant G/A;T snv 2.2E-05; 0.16 0.700 1.000 1 2012 2012