Variant (rsID / SNP)

rs17844309

rs17844309 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PCDHA7. Location: chromosome 5, position 140,214,995. The table records no clinical significance for this variant.

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Reference-table entries

PCDHA7Not classified

Variant type: missense_variant
Chromosome / position: 5:140214995
HGVS: NM_018910.3,c.1027G>A,p.Val343Ile
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.