AXIN2, axin 2, 8313

N. diseases: 169; N. variants: 34
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121908567
rs121908567
1.000 0.080 17 65536345 stop gained C/A;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs1299440644
rs1299440644
1.000 0.160 17 65534008 frameshift variant A/- delins 4.0E-06
Oligodontia-Colorectal Cancer Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Stomatognathic Diseases 0.700 0
dbSNP: rs1555577613
rs1555577613
1.000 0.160 17 65537390 frameshift variant T/- del
Oligodontia-Colorectal Cancer Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Stomatognathic Diseases 0.700 0
dbSNP: rs1555577625
rs1555577625
1.000 0.160 17 65537399 frameshift variant C/- delins
Oligodontia-Colorectal Cancer Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Stomatognathic Diseases 0.700 0
dbSNP: rs1555583659
rs1555583659
1.000 0.160 17 65558426 frameshift variant CG/- del
Oligodontia-Colorectal Cancer Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Stomatognathic Diseases 0.700 0
dbSNP: rs1567754914
rs1567754914
1.000 0.160 17 65536954 frameshift variant G/- del
Oligodontia-Colorectal Cancer Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Stomatognathic Diseases 0.700 0
dbSNP: rs1567755946
rs1567755946
0.925 0.080 17 65537563 frameshift variant -/CGCGGGAGGCAGC delins
CUI: C4082304
Disease: Oligodontia
Oligodontia
0.700 0
dbSNP: rs1567755946
rs1567755946
0.925 0.080 17 65537563 frameshift variant -/CGCGGGAGGCAGC delins
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs1567769335
rs1567769335
1.000 0.160 17 65558387 stop gained C/T snv
Oligodontia-Colorectal Cancer Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Stomatognathic Diseases 0.700 0
dbSNP: rs267606674
rs267606674
0.925 0.160 17 65536467 frameshift variant C/-;CC delins
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs267606674
rs267606674
0.925 0.160 17 65536467 frameshift variant C/-;CC delins
Oligodontia-Colorectal Cancer Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Stomatognathic Diseases 0.700 0
dbSNP: rs367624903
rs367624903
1.000 0.160 17 65537394 stop gained C/A;T snv 4.0E-06 7.0E-06
Oligodontia-Colorectal Cancer Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Stomatognathic Diseases 0.700 0
dbSNP: rs730882193
rs730882193
0.807 0.200 17 65536472 stop gained C/G;T snv
Oligodontia-Colorectal Cancer Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Stomatognathic Diseases 0.700 0
dbSNP: rs771001164
rs771001164
1.000 0.160 17 65537821 frameshift variant CTCT/-;CT delins 5.4E-06 7.0E-06
Oligodontia-Colorectal Cancer Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Stomatognathic Diseases 0.700 0
dbSNP: rs12452505
rs12452505
17 65560284 5 prime UTR variant C/G snv 0.10
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs4790930
rs4790930
17 65555266 intron variant C/A snv 0.66
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs1133683
rs1133683
1.000 0.080 17 65537650 synonymous variant G/A snv 0.60; 5.4E-06 0.53
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs1133683
rs1133683
1.000 0.080 17 65537650 synonymous variant G/A snv 0.60; 5.4E-06 0.53
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs1133683
rs1133683
1.000 0.080 17 65537650 synonymous variant G/A snv 0.60; 5.4E-06 0.53
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs121908568
rs121908568
0.807 0.160 17 65536495 stop gained G/A snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 1.000 1 2004 2004
dbSNP: rs121908568
rs121908568
0.807 0.160 17 65536495 stop gained G/A snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs121908568
rs121908568
0.807 0.160 17 65536495 stop gained G/A snv
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2016 2016
dbSNP: rs121908568
rs121908568
0.807 0.160 17 65536495 stop gained G/A snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.010 1.000 1 2004 2004
dbSNP: rs121908568
rs121908568
0.807 0.160 17 65536495 stop gained G/A snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs121908568
rs121908568
0.807 0.160 17 65536495 stop gained G/A snv
CUI: C0000846
Disease: Agenesis
Agenesis
0.010 1.000 1 2016 2016