Variant (rsID / SNP)

rs177252

rs177252 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CATSPER3. Location: chromosome 5, position 134,343,799. The table records no clinical significance for this variant.

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Reference-table entries

CATSPER3Not classified

Variant type: synonymous_variant
Chromosome / position: 5:134343799
HGVS: NM_178019.3,c.645A>G,p.Ala215Ala
Allele change: Synonymous_A215A

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.