Variant (rsID / SNP)

rs4635850

rs4635850 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDLIM3. Location: chromosome 4, position 186,423,637. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

PDLIM3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:186423637
Cytoband: 4q35.1
HGVS: NM_014476.6(PDLIM3):c.906C>T (p.Val302=)
Allele change: Synonymous_V254V

Associated conditions / phenotypes

Cardiovascular phenotype|Primary dilated cardiomyopathy|Hypertrophic cardiomyopathy

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.