GRN, granulin precursor, 2896

N. diseases: 412; N. variants: 66
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63751243
rs63751243
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C1843792
Disease:
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
0.800 GeneticVariation UNIPROT
dbSNP: rs63751243
rs63751243
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C1843792
Disease:
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
A 0.800 CausalMutation CLINVAR
dbSNP: rs1392550887
rs1392550887
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C3539123
Disease:
CEROID LIPOFUSCINOSIS, NEURONAL, 11
GC 0.700 CausalMutation CLINVAR
dbSNP: rs1392550887
rs1392550887
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C1843792
Disease:
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
GC 0.700 CausalMutation CLINVAR
dbSNP: rs1555611256
rs1555611256
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C1843792
Disease:
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
C 0.700 CausalMutation CLINVAR
dbSNP: rs1567885658
rs1567885658
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C0338451
Disease:
Frontotemporal dementia
CT 0.700 CausalMutation CLINVAR
dbSNP: rs1567885728
rs1567885728
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C0002395
Disease:
Alzheimer's Disease
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1567886206
rs1567886206
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C0338451
Disease:
Frontotemporal dementia
TA 0.700 CausalMutation CLINVAR
dbSNP: rs1567886445
rs1567886445
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C0338451
Disease:
Frontotemporal dementia
TTGTGAAGACAGGGTGCACTGCTGTC 0.700 CausalMutation CLINVAR
dbSNP: rs1567886478
rs1567886478
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C0338451
Disease:
Frontotemporal dementia
C 0.700 CausalMutation CLINVAR
dbSNP: rs1567887015
rs1567887015
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C0338451
Disease:
Frontotemporal dementia
TA 0.700 CausalMutation CLINVAR
dbSNP: rs1567887496
rs1567887496
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C1843792
Disease:
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
T 0.700 CausalMutation CLINVAR
dbSNP: rs1567887496
rs1567887496
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C3539123
Disease:
CEROID LIPOFUSCINOSIS, NEURONAL, 11
T 0.700 CausalMutation CLINVAR
dbSNP: rs1567887777
rs1567887777
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C0338451
Disease:
Frontotemporal dementia
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1567888461
rs1567888461
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C0338451
Disease:
Frontotemporal dementia
A 0.700 CausalMutation CLINVAR
dbSNP: rs193026789
rs193026789
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C0338451
Disease:
Frontotemporal dementia
A 0.700 CausalMutation CLINVAR
dbSNP: rs606231220
rs606231220
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C1843792
Disease:
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
GCTGC 0.700 CausalMutation CLINVAR
dbSNP: rs606231221
rs606231221
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C1843792
Disease:
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
A 0.700 CausalMutation CLINVAR
dbSNP: rs63749801
rs63749801
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C1843792
Disease:
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
T 0.700 CausalMutation CLINVAR
dbSNP: rs63749801
rs63749801
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C0338451
Disease:
Frontotemporal dementia
T 0.700 CausalMutation CLINVAR
dbSNP: rs63749817
rs63749817
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C0338451
Disease:
Frontotemporal dementia
A 0.700 CausalMutation CLINVAR
dbSNP: rs63749817
rs63749817
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C1843792
Disease:
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
A 0.700 CausalMutation CLINVAR
dbSNP: rs63749877
rs63749877
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C3539123
Disease:
CEROID LIPOFUSCINOSIS, NEURONAL, 11
C 0.700 CausalMutation CLINVAR
dbSNP: rs63749877
rs63749877
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C0282513
Disease:
Primary Progressive Aphasia (disorder)
C 0.700 CausalMutation CLINVAR
dbSNP: rs63749877
rs63749877
Entrez Id: 2896
Gene Symbol: GRN
GRN
CUI: C1843792
Disease:
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
C 0.700 CausalMutation CLINVAR