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: rs10490571
rs10490571
5 0.827 0.320 2 102100877 intron variant C/T snv 0.29 0.010 1.000 1 2019 2019
dbSNP: rs956730
rs956730
2 0.925 0.120 2 102141656 intron variant G/A snv 0.42 0.010 1.000 1 2019 2019