Variant (rsID / SNP)
rs267606723
rs267606723 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CFTR. Location: chromosome 7, position 117,282,505. The table records no clinical significance for this variant.
Reference-table entries
CFTRNot classified
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:117282505
- Cytoband
- 7q31.2
- HGVS
- NM_000492.4(CFTR):c.3731G>T (p.Gly1244Val)
- Allele change
- Missense_G1244V
Associated conditions / phenotypes
Cystic fibrosis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.