Variant (rsID / SNP)
rs2271613
rs2271613 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH17. Location: chromosome 17, position 76,423,097. Clinical significance in the table: Benign.
Reference-table entries
DNAH17Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:76423097
- Cytoband
- 17q25.3
- HGVS
- NM_173628.4(DNAH17):c.12681C>T (p.Tyr4227=)
- Allele change
- Synonymous_Y4227Y
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.