Variant (rsID / SNP)

rs164076

rs164076 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PCDH12. Location: chromosome 5, position 141,337,126. The table records no clinical significance for this variant.

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Reference-table entries

PCDH12Not classified

Variant type: synonymous_variant
Chromosome / position: 5:141337126
HGVS: NM_016580.4,c.291G>A,p.Leu97Leu
Allele change: Synonymous_L97L

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.