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: rs1048303
rs1048303
1 7 101160859 3 prime UTR variant C/T snv 0.54 0.700 1.000 1 2019 2019
dbSNP: rs2074683
rs2074683
1 7 101160333 intron variant C/T snv 0.54 0.700 1.000 1 2019 2019