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: rs11071559
rs11071559
4 0.925 0.080 15 60777789 intron variant C/T snv 0.23 0.700 1.000 2 2019 2019