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: rs10998022
rs10998022
2 0.925 0.040 10 68210229 intron variant C/T snv 0.26 0.700 1.000 1 2007 2007