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: rs2075672
rs2075672
8 7 100642673 intron variant A/G snv 0.65 0.800 1.000 2 2012 2016
dbSNP: rs1052897
rs1052897
1 7 100643148 3 prime UTR variant A/T snv 0.88 0.700 1.000 1 2012 2012