Variant (rsID / SNP)
rs10783071
rs10783071 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRDT. Location: chromosome 1, position 92,428,495. The table records no clinical significance for this variant.
Reference-table entries
BRDTNot classified
- Variant type
- missense_variant
- Chromosome / position
- 1:92428495
- HGVS
- NM_001242806.2,c.184C>A,p.Gln62Lys
- Allele change
- Missense_Q62K
Associated conditions / phenotypes
Azoospermia|Infertility
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.