Variant (rsID / SNP)

rs387906697

rs387906697 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TGFBR1. Location: chromosome 9, position 101,908,876. Clinical significance in the table: Pathogenic.

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Reference-table entries

TGFBR1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 9:101908876
Cytoband: 9q22.33
HGVS: NM_004612.4(TGFBR1):c.1240C>T (p.Arg414Ter)
Allele change: Nonsense_R337X

Associated conditions / phenotypes

Multiple self-healing squamous epithelioma|Familial thoracic aortic aneurysm and aortic dissection

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.