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: rs10274928
rs10274928
1 7 28102469 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs702814
rs702814
2 1.000 0.080 7 28133113 intron variant C/T snv 0.37 0.700 1.000 1 2019 2019