"Ambry Genetics"[submitter] AND "SNRPG"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2555872	NM_003096.4(SNRPG):c.155G>T (p.Gly52Val)	SNRPG (G34V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3167059	NM_003096.4(SNRPG):c.76C>G (p.His26Asp)	SNRPG (H14D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3167058	NM_003096.4(SNRPG):c.33A>G (p.Lys11=)	SNRPG	Single nucleotide variant (synonymous variant +2 more)	not specified	GLikely benign

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