Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs587782895
rs587782895
1.000 0.200 5 132604020 frameshift variant AA/- del 5.6E-05
Nijmegen Breakage Syndrome-Like Disorder
0.700 1.000 1 2016 2016
dbSNP: rs587782895
rs587782895
1.000 0.200 5 132604020 frameshift variant AA/- del 5.6E-05
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 1.000 1 2016 2016