List of variants in gene ALB reported as pathogenic for hematologic disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000477.7(ALB):c.412C>T (p.Arg138Ter)	rs77238412	0.00002
NM_000477.7(ALB):c.102_108del	rs750893435
NM_000477.7(ALB):c.1098dup (p.Val367fs)	rs1577939845
NM_000477.7(ALB):c.166C>T (p.Gln56Ter)	rs75470261
NM_000477.7(ALB):c.714-2A>G	rs77335374
NM_000477.7(ALB):c.714G>A (p.Trp238Ter)	rs76454301
NM_000477.7(ALB):c.872dup (p.Asn291fs)	rs77449454

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