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: rs7709909
rs7709909
1 1.000 0.080 5 80705351 intron variant C/T snv 0.34 0.700 1.000 1 2018 2018