Variant (rsID / SNP)
rs121918346
rs121918346 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DAZL. Location: chromosome 3, position 16,639,676. Clinical significance in the table: risk factor.
Reference-table entries
DAZLRisk factor
- Clinical significance (as recorded)
- risk factor
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:16639676
- Cytoband
- 3p24.3
- HGVS
- NM_001351.4(DAZL):c.160A>G (p.Thr54Ala)
- Allele change
- Missense_T54A
Associated conditions / phenotypes
Spermatogenic failure, susceptibility to
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.