Variant (rsID / SNP)

rs1064796072

rs1064796072 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BMPR1A. Location: chromosome 10, position 88,676,890. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

BMPR1ALikely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: Deletion
Chromosome / position: 10:88676890
Cytoband: 10q23.2
HGVS: NM_004329.2(BMPR1A):c.676delG

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.