Variant (rsID / SNP)

rs397516371

rs397516371 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TPM1. Location: chromosome 15, position 63,351,810. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

TPM1Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 15:63351810
Cytoband: 15q22.2
HGVS: NM_001018005.2(TPM1):c.423G>C (p.Met141Ile)
Allele change: Missense_M141I

Associated conditions / phenotypes

Primary dilated 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.