Variant (rsID / SNP)

rs61323727

rs61323727 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCB7. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ABCB7Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Cytoband: Xq13.3
HGVS: NM_001271696.3(ABCB7):c.246+1G>A
Allele change: Silent

Associated conditions / phenotypes

Sideroblastic Anemia and Ataxia

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.