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: rs12452505
rs12452505
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs4790930
rs4790930
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs121908568
rs121908568
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C1837750
Disease:
Oligodontia-Colorectal Cancer Syndrome
A 0.700 CausalMutation CLINVAR Functional analysis of a novel missense mutation in AXIN2 associated with non-syndromic tooth agenesis. 27090353 2016
dbSNP: rs121908568
rs121908568
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C1837750
Disease:
Oligodontia-Colorectal Cancer Syndrome
A 0.700 CausalMutation CLINVAR Mutations in WNT10A are present in more than half of isolated hypodontia cases. 22581971 2012
dbSNP: rs773157765
rs773157765
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C1837750
Disease:
Oligodontia-Colorectal Cancer Syndrome
T 0.700 GeneticVariation CLINVAR AXIN2-associated autosomal dominant ectodermal dysplasia and neoplastic syndrome. 21416598 2011
dbSNP: rs775783026
rs775783026
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C1837750
Disease:
Oligodontia-Colorectal Cancer Syndrome
C 0.700 GeneticVariation CLINVAR AXIN2-associated autosomal dominant ectodermal dysplasia and neoplastic syndrome. 21416598 2011
dbSNP: rs978837790
rs978837790
Entrez Id: 8313
Gene Symbol: AXIN2
AXIN2
CUI: C1837750
Disease:
Oligodontia-Colorectal Cancer Syndrome
C 0.700 GeneticVariation CLINVAR AXIN2-associated autosomal dominant ectodermal dysplasia and neoplastic syndrome. 21416598 2011
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: 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