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: rs1169310
rs1169310
3 12 121001630 3 prime UTR variant G/A snv 0.31 0.700 1.000 1 2011 2011
dbSNP: rs1169313
rs1169313
6 12 121004867 intron variant T/A;C snv 0.700 1.000 1 2011 2011