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: rs13082914
rs13082914
1 1.000 0.040 3 156287165 intron variant C/T snv 0.29 0.700 1.000 1 2016 2016