Variant (rsID / SNP)

rs11167743

rs11167743 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PCDHB9. Location: chromosome 5, position 140,567,608. The table records no clinical significance for this variant.

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Reference-table entries

PCDHB9Not classified

Variant type: missense_variant
Chromosome / position: 5:140567608
HGVS: NM_019119.5,c.716C>T,p.Ala239Val
Allele change: Missense_A239V

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.