Variant (rsID / SNP)
rs35258161
rs35258161 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GLMN. Location: chromosome 1, position 92,733,663. Clinical significance in the table: Benign.
Reference-table entries
GLMNBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:92733663
- Cytoband
- 1p22.1
- HGVS
- NM_053274.3(GLMN):c.1007T>C (p.Leu336Ser)
- Allele change
- Silent
Associated conditions / phenotypes
Glomuvenous malformation
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.