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: rs13331259
rs13331259
14 16 249924 intron variant A/G snv 3.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs76792961
rs76792961
13 16 243594 intron variant C/T snv 7.3E-03 0.700 1.000 1 2019 2019