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: rs3758539
rs3758539
4 0.925 0.120 10 93601831 intron variant C/T snv 0.13 0.020 0.500 2 2014 2016
dbSNP: rs34571439
rs34571439
1 10 93591553 intron variant A/C snv 0.24 0.010 1.000 1 2014 2014
dbSNP: rs7091052
rs7091052
1 10 93595641 intron variant G/A snv 0.15 0.010 1.000 1 2019 2019