Variant (rsID / SNP)
rs61731638
rs61731638 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH1. Location: chromosome 3, position 52,422,300. Clinical significance in the table: Benign.
Reference-table entries
DNAH1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:52422300
- Cytoband
- 3p21.1
- HGVS
- NM_015512.5(DNAH1):c.9121C>T (p.Arg3041Cys)
- Allele change
- Missense_R3041C
Associated conditions / phenotypes
Spermatogenic failure 18|Ciliary dyskinesia, primary, 37
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.