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: rs7756881
rs7756881
1 1.000 0.040 6 26389698 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs9461249
rs9461249
1 1.000 0.040 6 26383158 5 prime UTR variant T/C snv 0.23 0.700 1.000 1 2012 2012