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: rs10668
rs10668
1 3 123492217 3 prime UTR variant G/T snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs16834431
rs16834431
1 3 123567009 intron variant C/T snv 0.19 0.700 1.000 1 2019 2019