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: rs1751242
rs1751242
1 9 110879503 intron variant T/A snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs547116
rs547116
1 9 110877852 intron variant T/A snv 0.40 0.700 1.000 1 2016 2016
dbSNP: rs551517
rs551517
2 9 110874513 3 prime UTR variant C/T snv 0.27 0.700 1.000 1 2016 2016