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Variant (rsID / SNP)

rs10747493

BRDT

rs10747493 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRDT. Location: chromosome 1, position 92,457,843. The table records no clinical significance for this variant.

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Reference-table entries

BRDTNot classified
Variant type
missense_variant
Chromosome / position
1:92457843
HGVS
NM_001242806.2,c.2099C>T,p.Pro700Leu
Allele change
Missense_P650L

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.