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: rs1616727
rs1616727
1 9 108935147 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2275641
rs2275641
1 9 108934109 5 prime UTR variant G/A;C snv 0.700 1.000 1 2018 2018