Variant (rsID / SNP)
rs142111745
rs142111745 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIM37. Location: chromosome 17, position 57,075,902. Clinical significance in the table: Uncertain significance.
Reference-table entries
TRIM37Uncertain significance
- Clinical significance (as recorded)
- Uncertain significance
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:57075902
- Cytoband
- 17q22
- HGVS
- NM_015294.6(TRIM37):c.*836A>G
- Allele change
- Silent
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.