Variant (rsID / SNP)

rs3733709

rs3733709 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PCDHA3. Location: chromosome 5, position 140,181,648. The table records no clinical significance for this variant.

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Reference-table entries

PCDHA3Not classified

Variant type: missense_variant
Chromosome / position: 5:140181648
HGVS: NM_018906.3,c.866T>C,p.Ile289Thr
Allele change: Silent

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.