Variant (rsID / SNP)
rs6935293
rs6935293 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH8. Location: chromosome 6, position 38,704,943. Clinical significance in the table: Benign.
Reference-table entries
DNAH8Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 6:38704943
- Cytoband
- 6p21.2
- HGVS
- NM_001206927.2(DNAH8):c.863A>G (p.Asn288Ser)
- Allele change
- Missense_N71S
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.