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: rs7233634
rs7233634
1 18 27137739 intron variant T/C snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs9952639
rs9952639
1 18 27129640 intron variant G/C snv 0.32 0.700 1.000 1 2018 2018