Related gene-specific medical variations for Gene (Select 4507) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1223355	NM_002451.4(MTAP):c.33+142C>G	LOC130001599, MTAP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 29791	NC_000009.12:g.21931006A>G	ERVFRD-3, MTAP	Single nucleotide variant	Diaphyseal medullary stenosis-bone malignancy syndrome	GPathogenic
Select item 29790	NC_000009.12:g.21931079A>G	ERVFRD-3, MTAP	Single nucleotide variant	Diaphyseal medullary stenosis-bone malignancy syndrome	GPathogenic

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