ClinVar Miner

List of variants reported as uncertain significance for X-linked sideroblastic anemia with ataxia by Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard

Included ClinVar conditions (1):

X-linked sideroblastic anemia with ataxia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_001271696.3(ABCB7):c.1936-3C>G	rs1602330362

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