Variant (rsID / SNP)

rs55724801

rs55724801 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPATA16. Location: chromosome 3, position 172,766,777. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SPATA16Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:172766777
Cytoband: 3q26.31
HGVS: NM_031955.6(SPATA16):c.720G>A (p.Arg240=)
Allele change: Synonymous_R240R

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.