ClinVar for MedGen (Select 21548) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3238621	NM_002771.4(PRSS3):c.74T>C (p.Val25Ala)	PRSS3, UBE2R2-AS1 (V18A +2 more)	Single nucleotide variant (missense variant +1 more)	Thyroiditis	GUncertain significance
Select item 128688	NM_001807.6(CEL):c.1966G>C (p.Ala656Pro)	CEL (A656P)	Single nucleotide variant (missense variant)	Chronic kidney disease +11 more	GUncertain significance