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Variant (rsID / SNP)

rs45498797

CSRP3

rs45498797 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CSRP3. Location: chromosome 11, position 19,223,546. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

CSRP3Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:19223546
Cytoband
11p15.1
HGVS
NM_003476.4(CSRP3):c.-74A>C
Allele change
Silent

Associated conditions / phenotypes

Hypertrophic cardiomyopathy 12|Cardiomyopathy

Public references

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