Variant (rsID / SNP)
rs2235611
rs2235611 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SRSF6. Location: chromosome 20, position 42,089,511. The table records no clinical significance for this variant.
Reference-table entries
SRSF6Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 20:42089511
- HGVS
- NM_006275.6,c.843T>C,p.Pro281Pro
- Allele change
- Synonymous_P281P
Associated conditions / phenotypes
Scleroderma, Familial Progressive|Pulmonary Fibrosis|Interstitial Lung Disease|Lung Disease|Macular Degeneration, Age-Related, 1|Microvascular Complications of Diabetes 5|Microvascular Complications of Diabetes 2|Microvascular Complications of Diabetes 1|Eye Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.