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Variant (rsID / SNP)

rs146768859

PDLIM3

rs146768859 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDLIM3. Location: chromosome 4, position 186,456,560. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

PDLIM3Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
4:186456560
Cytoband
4q35.1
HGVS
NM_014476.6(PDLIM3):c.29C>T (p.Pro10Leu)
Allele change
Missense_P10L

Associated conditions / phenotypes

Primary dilated cardiomyopathy|Hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy

Public references

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