List of variants in gene RPSA reported as benign for Familial isolated congenital asplenia

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002295.6(RPSA):c.-8T>C	rs1803893	0.50177
NM_002295.6(RPSA):c.134-32C>T	rs3772138	0.26547
NM_002295.6(RPSA):c.519G>A (p.Leu173=)	rs2269350	0.26529

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