Related gene-specific medical variations for Gene (Select 107988023) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3029904	NM_001316352.2(PTH):c.-5G>A	LOC107988023, PTH	Single nucleotide variant (5 prime UTR variant)	PTH-related condition	GLikely benign
Select item 303706	NM_000315.4(PTH):c.-83T>C	LOC107988023, PTH	Single nucleotide variant (5 prime UTR variant +1 more)	Familial hypoparathyroidism	GUncertain significance
Select item 303705	NM_000315.4(PTH):c.-33C>T	LOC107988023, PTH	Single nucleotide variant (5 prime UTR variant +1 more)	Familial hypoparathyroidism	GUncertain significance

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