Variant (rsID / SNP)
rs7527925
rs7527925 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH14. Location: chromosome 1, position 225,534,219. Clinical significance in the table: Benign.
Reference-table entries
DNAH14Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:225534219
- Cytoband
- 1q42.12
- HGVS
- NM_001367479.1(DNAH14):c.11159T>C (p.Val3720Ala)
- Allele change
- Missense_V3627A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.