Variant (rsID / SNP)
rs225014
rs225014 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DIO2. Location: chromosome 14, position 80,669,580. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- missense_variant
- Chromosome / position
- 14:80669580
- HGVS
- NM_013989.5,c.274A>G,p.Thr92Ala
- Allele change
- Silent
Associated conditions / phenotypes
Graves' Disease|Kashin-Beck Disease|Hypothyroidism|Type 2 Diabetes Mellitus|Osteoarthritis|Thyroid Gland Disease|Alcohol Dependence|Myocardial Infarction|Diabetes Mellitus|Thyroid Carcinoma|Mild Cognitive Impairment|Stroke, Ischemic|Anxiety|Major Affective Disorder 5|Major Affective Disorder 8|Major Affective Disorder 9|Major Affective Disorder 6|Acute Myocardial Infarction
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.