Variant (rsID / SNP)
rs35871562
rs35871562 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIM37. Location: chromosome 17, position 57,105,984. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
TRIM37Benign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:57105984
- Cytoband
- 17q22
- HGVS
- NM_015294.6(TRIM37):c.2049C>T (p.Ala683=)
- Allele change
- Synonymous_A683A
Associated conditions / phenotypes
Mulibrey nanism syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.