List of variants in gene SRP54 reported as likely benign for leukopenia

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_003136.4(SRP54):c.1327+16_1327+32del	rs369856554	0.16649
NM_003136.4(SRP54):c.636A>C (p.Ile212=)	rs140228686	0.00113
NM_003136.4(SRP54):c.1008T>A (p.Phe336Leu)

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