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: rs3758538
rs3758538
2 1.000 0.080 10 93602293 intron variant T/G snv 0.18 0.010 1.000 1 2016 2016
dbSNP: rs3758539
rs3758539
4 0.925 0.120 10 93601831 intron variant C/T snv 0.13 0.010 1.000 1 2011 2011