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: rs7896783
rs7896783
3 10 63402393 intron variant G/A;C snv 0.800 1.000 1 2013 2013
dbSNP: rs7916868
rs7916868
3 10 63229171 intron variant A/T snv 0.47 0.700 1.000 2 2016 2017
dbSNP: rs10761756
rs10761756
1 10 63412568 intron variant C/T snv 0.42 0.700 1.000 1 2017 2017