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: rs3116150
rs3116150
1 1.000 0.080 16 31486700 intron variant G/A snv 0.18 0.010 1.000 1 2019 2019
dbSNP: rs3813008
rs3813008
1 1.000 0.080 16 31486560 intron variant G/A;C snv 0.010 1.000 1 2019 2019
dbSNP: rs9934336
rs9934336
1 1.000 0.080 16 31484552 intron variant G/A snv 0.24 0.010 < 0.001 1 2019 2019