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: rs12974777
rs12974777
1 1.000 0.040 19 18654853 intron variant C/T snv 0.46 0.700 1.000 1 2019 2019