Variant (rsID / SNP)
rs3856154
rs3856154 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH14. Location: chromosome 1, position 225,565,015. Clinical significance in the table: Benign.
Reference-table entries
DNAH14Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:225565015
- Cytoband
- 1q42.12
- HGVS
- NM_001367479.1(DNAH14):c.12593T>C (p.Leu4198Pro)
- Allele change
- Missense_L4096P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.