ClinVar for PMC (Select 2669787) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 565669	NM_001379610.1(SPINK1):c.-53C>T	SPINK1	Single nucleotide variant (5 prime UTR variant)	Hereditary pancreatitis +1 more	GUncertain significance
Select item 553627	NM_000525.4(KCNJ11):c.-54C>T	KCNJ11	Single nucleotide variant (5 prime UTR variant +1 more)	Permanent neonatal diabetes mellitus +6 more	GUncertain significance
Select item 15469	NC_000011.10:g.5227100T>C	HBB, LOC106099062 +1 more	Single nucleotide variant	not provided +11 more	GPathogenic

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