Variant (rsID / SNP)

rs7074064

rs7074064 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BMPR1A. Location: chromosome 10, position 88,683,122. Clinical significance in the table: Benign.

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Reference-table entries

BMPR1ABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:88683122
Cytoband: 10q23.2
HGVS: NM_004329.3(BMPR1A):c.1343-11T>C
Allele change: Silent

Associated conditions / phenotypes

Generalized juvenile polyposis/juvenile polyposis coli|Hereditary cancer-predisposing syndrome|Juvenile polyposis 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.