rs63749877, GRN

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
CEROID LIPOFUSCINOSIS, NEURONAL, 11
CUI: C3539123
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 11
8 0.882 0.120 17 44351139 frameshift variant CACT/- delins 0.700 0
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
CUI: C1843792
Disease: FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
23 0.882 0.120 17 44351139 frameshift variant CACT/- delins 0.700 0
Primary Progressive Aphasia (disorder)
CUI: C0282513
Disease: Primary Progressive Aphasia (disorder)
11 0.882 0.120 17 44351139 frameshift variant CACT/- delins 0.700 0