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: rs1140227
rs1140227
1 1 41028139 3 prime UTR variant C/T snv 0.10 0.700 1.000 1 2019 2019
dbSNP: rs12736566
rs12736566
1 1 41018479 intron variant T/G snv 1.9E-02 0.700 1.000 1 2018 2018