List of variants in gene ABCB4 reported as uncertain significance for retinal disorder

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_000443.4(ABCB4):c.2800G>A (p.Ala934Thr)	rs61730509	0.00389
NM_000443.4(ABCB4):c.1529A>G (p.Asn510Ser)	rs375315619	0.00009

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