Variant (rsID / SNP)
rs2279574
rs2279574 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DUSP6. Location: chromosome 12, position 89,745,477. Clinical significance in the table: Benign.
Reference-table entries
DUSP6Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- missense_variant
- Chromosome / position
- 12:89745477
- HGVS
- NM_001946.4,c.340G>T,p.Val114Leu
- Allele change
- Missense_V114L
Associated conditions / phenotypes
Hypogonadotropic Hypogonadism 19 with or Without Anosmia|Squamous Cell Carcinoma|Lung Squamous Cell Carcinoma|Major Affective Disorder 8|Lung Cancer|Major Affective Disorder 9|Bipolar Disorder
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.