Variant (rsID / SNP)

rs145703021

rs145703021 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMPO. Location: chromosome 12, position 98,927,344. Clinical significance in the table: Benign/Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TMPOBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 12:98927344
Cytoband: 12q23.1
HGVS: NM_001032283.3(TMPO):c.565+1728G>C
Allele change: Silent

Associated conditions / phenotypes

Loeys-Dietz syndrome 2|Cardiovascular phenotype|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.