Variant (rsID / SNP)
rs61745597
rs61745597 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZGRF1. Location: chromosome 4, position 113,544,993. Clinical significance in the table: Benign.
Reference-table entries
ZGRF1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:113544993
- Cytoband
- 4q25
- HGVS
- NM_018392.5(ZGRF1):c.142C>A (p.Leu48Met)
- Allele change
- Missense_L48M
Associated conditions / phenotypes
Childhood apraxia of speech
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.