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: rs587782090
rs587782090
1.000 0.200 5 132587942 stop gained G/T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.700 0
dbSNP: rs587782090
rs587782090
1.000 0.200 5 132587942 stop gained G/T snv
Nijmegen Breakage Syndrome-Like Disorder
0.700 0