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: rs1501899
rs1501899
8 0.790 0.240 3 122188481 intron variant A/G snv 0.62 0.010 1.000 1 2017 2017
dbSNP: rs7652589
rs7652589
13 0.732 0.400 3 122170241 downstream gene variant A/G snv 0.60 0.010 1.000 1 2017 2017