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Variant (rsID / SNP)

rs2452600

PDLIM5

rs2452600 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDLIM5. Location: chromosome 4, position 95,496,882. The table records no clinical significance for this variant.

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Reference-table entries

PDLIM5Not classified
Variant type
missense_variant
Chromosome / position
4:95496882
HGVS
NM_001256428.2,c.41C>T,p.Ser14Phe
Allele change
Silent

Associated conditions / phenotypes

Mental Depression|Major Depressive Disorder|Depression

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.