Variant (rsID / SNP)

rs1803446

rs1803446 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TGFBR2. Location: chromosome 3, position 30,734,924. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

TGFBR2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:30734924
Cytoband: 3p24.1
HGVS: NM_003242.6(TGFBR2):c.*1833A>C
Allele change: Silent

Associated conditions / phenotypes

Familial thoracic aortic aneurysm and aortic dissection|Loeys-Dietz syndrome|Marfan syndrome

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.