Variant (rsID / SNP)

rs41265215

rs41265215 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TPM3. Location: chromosome 1, position 154,164,063. Clinical significance in the table: Likely benign.

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Reference-table entries

TPM3Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:154164063
Cytoband: 1q21.3
HGVS: NM_152263.4(TPM3):c.118-276T>C
Allele change: Silent

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.