ClinVar Miner

List of variants in gene SRP19 studied for Shwachman-Diamond syndrome 1; Severe congenital neutropenia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_003135.3(SRP19):c.189+5G>A	rs1322282571

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