Variant (rsID / SNP)

rs886038847

rs886038847 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TGFBR2. Location: chromosome 3, position 30,713,811. Clinical significance in the table: Pathogenic.

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Reference-table entries

TGFBR2Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 3:30713811
Cytoband: 3p24.1
HGVS: NM_003242.6(TGFBR2):c.1136A>T (p.Asp379Val)
Allele change: Missense_D379V

Associated conditions / phenotypes

Cardiovascular phenotype

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.