ClinVar Miner

List of variants in gene combination APOB, APOB3'MAR reported as uncertain significance for autosomal recessive metabolic cerebellar ataxia

Included ClinVar conditions (9):

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

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000384.3(APOB):c.*207C>A	rs886055566	0.00001
NM_000384.3(APOB):c.13601A>G (p.Tyr4534Cys)	rs886055571	0.00001

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