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Variant (rsID / SNP)

rs200537780

BMPR1A

rs200537780 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BMPR1A. Location: chromosome 10, position 88,676,886. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

BMPR1ABenign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
10:88676886
Cytoband
10q23.2
HGVS
NM_004329.3(BMPR1A):c.676-5T>C
Allele change
Silent

Associated conditions / phenotypes

Generalized juvenile polyposis/juvenile polyposis coli|Hereditary cancer-predisposing syndrome|Juvenile polyposis syndrome|Polyposis syndrome, hereditary mixed, 2

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.