ClinVar Miner

List of variants in gene combination ABCA1, LOC121331340 reported as uncertain significance for obsolete apolipoprotein A-I deficiency

Included ClinVar conditions (3):

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: 1

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HGVS	dbSNP	gnomAD frequency
NM_005502.4(ABCA1):c.4084C>T (p.Leu1362Phe)	rs1364173135

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