Variant (rsID / SNP)

rs367543032

rs367543032 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BLM. Location: chromosome 15, position 91,337,568. Clinical significance in the table: Uncertain significance.

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Reference-table entries

BLMUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 15:91337568
Cytoband: 15q26.1
HGVS: NM_000057.4(BLM):c.3191A>G (p.Asp1064Gly)
Allele change: Missense_D689V

Associated conditions / phenotypes

Bloom syndrome|Hereditary cancer-predisposing 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.