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: rs7606512
rs7606512
9 0.790 0.080 2 234701030 intron variant C/T snv 0.11 0.700 1.000 1 2017 2017