C0685889[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 403395	NM_002295.6(RPSA):c.-8T>C	RPSA	Single nucleotide variant (5 prime UTR variant)	not provided +2 more	GBenign
Select item 1327975	NM_002295.6(RPSA):c.134-32C>T	RPSA	Single nucleotide variant (intron variant)	Familial isolated congenital asplenia +1 more	GBenign
Select item 403396	NM_002295.6(RPSA):c.519G>A (p.Leu173=)	RPSA	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign

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