Variant (rsID / SNP)

rs886038919

rs886038919 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TGFBR1. Location: chromosome 9, position 101,900,323. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

TGFBR1Pathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 9:101900323
Cytoband: 9q22.33
HGVS: NM_004612.4(TGFBR1):c.757A>G (p.Met253Val)
Allele change: Missense_M176V

Associated conditions / phenotypes

Cardiovascular phenotype|Loeys-Dietz syndrome|Familial thoracic aortic aneurysm and aortic dissection|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.