Variant (rsID / SNP)
rs4072037
rs4072037 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC1. Location: chromosome 1, position 155,162,067. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- synonymous_variant
- Chromosome / position
- 1:155162067
- HGVS
- NM_001371720.1,c.93G>A,p.Thr31Thr
- Allele change
- Synonymous_T31T
Associated conditions / phenotypes
Gastric Cancer|Lung Disease|Interstitial Lung Disease 2|Antisynthetase Syndrome|Pulmonary Fibrosis|Pulmonary Alveolar Proteinosis|Adenocarcinoma|Helicobacter Pylori Infection|Gastritis|Lung Cancer Susceptibility 3|Gastric Adenocarcinoma|Squamous Cell Carcinoma|Alcohol Dependence|Cardia Cancer|Ovarian Cancer|Scleroderma, Familial Progressive|Interstitial Lung Disease|Stomach Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.