Variant (rsID / SNP)
rs77298044
rs77298044 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PCK2, NRL. Location: chromosome 14, position 24,563,620. Clinical significance in the table: Benign.
Reference-table entries
PCK2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 14:24563620
- Cytoband
- 14q11.2
- HGVS
- NM_004563.4(PCK2):c.6C>T (p.Ala2=)
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.