List of variants in gene ALB reported as not provided

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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: 19

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HGVS	dbSNP	gnomAD frequency
NM_000477.7(ALB):c.1669G>A (p.Val557Met)	rs78284052	0.00017
NM_000477.7(ALB):c.228_229del (p.Val78fs)	rs75152012	0.00005
NM_000477.7(ALB):c.1300C>T (p.Arg434Cys)	rs78575701	0.00002
NM_000477.7(ALB):c.412C>T (p.Arg138Ter)	rs77238412	0.00002
NM_000477.7(ALB):c.1013A>G (p.Asp338Gly)	rs76242087
NM_000477.7(ALB):c.1013A>T (p.Asp338Val)	rs76242087
NM_000477.7(ALB):c.1195G>C (p.Asp399His)	rs77514449
NM_000477.7(ALB):c.1275C>A (p.Tyr425Ter)	rs281860283
NM_000477.7(ALB):c.1428+2T>C	rs78784172
NM_000477.7(ALB):c.1610del (p.Ile537fs)	rs77081291
NM_000477.7(ALB):c.166C>T (p.Gln56Ter)	rs75470261
NM_000477.7(ALB):c.1721A>C (p.Asp574Ala)	rs79738788
NM_000477.7(ALB):c.1750A>G (p.Lys584Glu)	rs76671808
NM_000477.7(ALB):c.1786-15T>A	rs78342924
NM_000477.7(ALB):c.1794dup (p.Leu599fs)	rs75000326
NM_000477.7(ALB):c.437T>A (p.Val146Glu)	rs77752336
NM_000477.7(ALB):c.597T>A (p.Ala199=)	rs281860282
NM_000477.7(ALB):c.714G>A (p.Trp238Ter)	rs76454301
NM_000477.7(ALB):c.802G>T (p.Glu268Ter)	rs78340021

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