Variant (rsID / SNP)

rs1052763

rs1052763 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSSK2, ESS2. Location: chromosome 22, position 19,119,751. The table records no clinical significance for this variant.

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Reference-table entries

TSSK2Not classified

Variant type: missense_variant
Chromosome / position: 22:19119751
HGVS: NM_053006.5,c.839C>T,p.Thr280Met
Allele change: Silent

Associated conditions / phenotypes

Azoospermia|Infertility

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.