Variant (rsID / SNP)

rs8666

rs8666 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PHPT1. Location: chromosome 9, position 139,744,524. The table records no clinical significance for this variant.

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Reference-table entries

PHPT1Not classified

Variant type: synonymous_variant
Chromosome / position: 9:139744524
HGVS: NM_001287342.2,c.226C>T,p.Leu76Leu
Allele change: Synonymous_L76L

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.