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: rs9719461
rs9719461
1 1.000 0.040 7 593078 intron variant C/T snv 0.72 0.700 1.000 1 2018 2018