Variant (rsID / SNP)

rs115095786

rs115095786 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPATA16. Location: chromosome 3, position 172,631,512. Clinical significance in the table: Likely benign.

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Reference-table entries

SPATA16Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:172631512
Cytoband: 3q26.31
HGVS: NM_031955.6(SPATA16):c.1526C>T (p.Ala509Val)
Allele change: Missense_A509V

Associated conditions / phenotypes

Globozoospermia

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.