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: rs7317038
rs7317038
1 13 113358583 intron variant C/T snv 0.34 0.800 1.000 1 2011 2011
dbSNP: rs4907622
rs4907622
3 13 113362571 intron variant G/C;T snv 0.700 1.000 1 2016 2016