Related gene-specific medical variations for Gene (Select 8434) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3152831	NM_021111.3(RECK):c.80G>T (p.Gly27Val)	LOC130001741, RECK (G27V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2608057	NM_021111.3(RECK):c.95G>A (p.Ser32Asn)	LOC130001741, RECK (S32N)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2491853	NM_021111.3(RECK):c.61G>T (p.Val21Phe)	LOC130001741, RECK (V21F)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2274276	NM_021111.3(RECK):c.59G>T (p.Gly20Val)	LOC130001741, RECK (G20V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance

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