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: rs16891982
rs16891982
13 0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 0.710 1.000 2 2009 2016
dbSNP: rs35407
rs35407
6 0.807 0.080 5 33946466 3 prime UTR variant A/C;G snv 0.700 1.000 1 2019 2019