Variant (rsID / SNP)
rs141055331
rs141055331 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZMYND10, RASSF1. Location: chromosome 3, position 50,379,974. Clinical significance in the table: Benign.
Reference-table entries
ZMYND10Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:50379974
- Cytoband
- 3p21.31
- HGVS
- NM_015896.4(ZMYND10):c.727C>T (p.Arg243Cys)
- Allele change
- Missense_R243C
Associated conditions / phenotypes
Primary ciliary dyskinesia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.