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: rs1046988
rs1046988
1 1 39753393 3 prime UTR variant C/G;T snv 0.33 0.31 0.700 1.000 1 2018 2018
dbSNP: rs12086750
rs12086750
1 1 39744796 intron variant G/C snv 0.31 0.700 1.000 1 2018 2018