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: rs10853525
rs10853525
1 18 44856687 intron variant C/T snv 0.35 0.700 1.000 1 2016 2016
dbSNP: rs991014
rs991014
2 18 44859921 intron variant C/T snv 0.35 0.700 1.000 1 2016 2016