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: rs10970975
rs10970975
1 9 32431933 intron variant A/G snv 0.34 0.700 1.000 1 2019 2019
dbSNP: rs7045087
rs7045087
3 9 32455264 downstream gene variant T/C snv 0.33 0.700 1.000 1 2016 2016