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: rs56388170
rs56388170
5 7 28684757 intron variant G/T snv 0.37 0.700 1.000 1 2016 2016
dbSNP: rs886816
rs886816
1 7 28683790 intron variant G/A snv 0.22 0.700 1.000 1 2018 2018