AXIN2, axin 2, 8313

N. diseases: 169; N. variants: 34
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908567
rs121908567
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C0009402
Disease:
Colorectal Carcinoma 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1299440644
rs1299440644
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C1837750
Disease:
Oligodontia-Colorectal Cancer Syndrome 		G 0.700 CausalMutation CLINVAR
dbSNP: rs1555577613
rs1555577613
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C1837750
Disease:
Oligodontia-Colorectal Cancer Syndrome 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1555577625
rs1555577625
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C1837750
Disease:
Oligodontia-Colorectal Cancer Syndrome 		G 0.700 CausalMutation CLINVAR
dbSNP: rs1555583659
rs1555583659
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C1837750
Disease:
Oligodontia-Colorectal Cancer Syndrome 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1567754914
rs1567754914
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C1837750
Disease:
Oligodontia-Colorectal Cancer Syndrome 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1567755946
rs1567755946
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C0009402
Disease:
Colorectal Carcinoma 		GGCCGCGGGAGGCA 0.700 CausalMutation CLINVAR
dbSNP: rs1567755946
rs1567755946
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C4082304
Disease:
Oligodontia 		GGCCGCGGGAGGCA 0.700 CausalMutation CLINVAR
dbSNP: rs1567769335
rs1567769335
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C1837750
Disease:
Oligodontia-Colorectal Cancer Syndrome 		T 0.700 CausalMutation CLINVAR
dbSNP: rs267606674
rs267606674
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C0009402
Disease:
Colorectal Carcinoma 		G 0.700 CausalMutation CLINVAR
dbSNP: rs267606674
rs267606674
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C1837750
Disease:
Oligodontia-Colorectal Cancer Syndrome 		G 0.700 CausalMutation CLINVAR
dbSNP: rs267606674
rs267606674
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C1837750
Disease:
Oligodontia-Colorectal Cancer Syndrome 		GC 0.700 CausalMutation CLINVAR
dbSNP: rs367624903
rs367624903
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C1837750
Disease:
Oligodontia-Colorectal Cancer Syndrome 		A 0.700 CausalMutation CLINVAR
dbSNP: rs730882193
rs730882193
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C1837750
Disease:
Oligodontia-Colorectal Cancer Syndrome 		T 0.700 CausalMutation CLINVAR
dbSNP: rs771001164
rs771001164
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C1837750
Disease:
Oligodontia-Colorectal Cancer Syndrome 		C 0.700 CausalMutation CLINVAR
dbSNP: rs121908568
rs121908568
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C1837750
Disease:
Oligodontia-Colorectal Cancer Syndrome 		A 0.700 CausalMutation CLINVAR Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer. 15042511 2004
dbSNP: rs773157765
rs773157765
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C1837750
Disease:
Oligodontia-Colorectal Cancer Syndrome 		T 0.700 GeneticVariation CLINVAR Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer. 15042511 2004
dbSNP: rs775783026
rs775783026
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C1837750
Disease:
Oligodontia-Colorectal Cancer Syndrome 		C 0.700 GeneticVariation CLINVAR Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer. 15042511 2004
dbSNP: rs978837790
rs978837790
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C1837750
Disease:
Oligodontia-Colorectal Cancer Syndrome 		C 0.700 GeneticVariation CLINVAR Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer. 15042511 2004
dbSNP: rs121908568
rs121908568
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C0020608
Disease:
Hypodontia 		0.020 GeneticVariation BEFREE We show that oligodontia and predisposition to cancer are caused by a nonsense mutation, Arg656Stop, in the Wnt-signaling regulator AXIN2. 15042511 2004
dbSNP: rs121908568
rs121908568
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C4082304
Disease:
Oligodontia 		0.020 GeneticVariation BEFREE We show that oligodontia and predisposition to cancer are caused by a nonsense mutation, Arg656Stop, in the Wnt-signaling regulator AXIN2. 15042511 2004
dbSNP: rs121908568
rs121908568
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C1306459
Disease:
Primary malignant neoplasm 		0.010 GeneticVariation BEFREE We show that oligodontia and predisposition to cancer are caused by a nonsense mutation, Arg656Stop, in the Wnt-signaling regulator AXIN2. 15042511 2004
dbSNP: rs121908568
rs121908568
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C0006826
Disease:
Malignant Neoplasms 		0.010 GeneticVariation BEFREE We show that oligodontia and predisposition to cancer are caused by a nonsense mutation, Arg656Stop, in the Wnt-signaling regulator AXIN2. 15042511 2004
dbSNP: rs2240308
rs2240308
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C0242379
Disease:
Malignant neoplasm of lung 		0.060 GeneticVariation BEFREE These results suggest that the AXIN2 Pro50Ser SNP is associated with development of lung cancer as a protective SNP, while an association between the AXIN2 SNP and risk of colorectal cancer and of head and neck cancer was not observed. 16820935 2006
dbSNP: rs2240308
rs2240308
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C0684249
Disease:
Carcinoma of lung 		0.060 GeneticVariation BEFREE These results suggest that the AXIN2 Pro50Ser SNP is associated with development of lung cancer as a protective SNP, while an association between the AXIN2 SNP and risk of colorectal cancer and of head and neck cancer was not observed. 16820935 2006