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: rs7746199
rs7746199
3 1.000 0.040 6 27293545 intron variant C/T snv 0.18 0.700 1.000 1 2017 2017