Variant (rsID / SNP)

rs940336

rs940336 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTCD1. Location: chromosome 7, position 99,032,458. The table records no clinical significance for this variant.

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Reference-table entries

PTCD1Not classified

Variant type: synonymous_variant
Chromosome / position: 7:99032458
HGVS: NM_015545.4,c.408G>A,p.Pro136Pro
Allele change: Synonymous_P136P

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.