Variant (rsID / SNP)

rs3733698

rs3733698 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PCDHB4. Location: chromosome 5, position 140,502,343. The table records no clinical significance for this variant.

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Reference-table entries

PCDHB4Not classified

Variant type: missense_variant
Chromosome / position: 5:140502343
HGVS: NM_018938.4,c.763C>T,p.Pro255Ser
Allele change: Missense_P255S

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.