Related gene-specific medical variations for Gene (Select 344901) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3207200	NM_198184.2(OSTN):c.205G>T (p.Val69Leu)	OSTN, OSTN-AS1 (V69L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2460910	NM_198184.2(OSTN):c.275A>T (p.Asp92Val)	OSTN, OSTN-AS1 (D92V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2330159	NM_198184.2(OSTN):c.272T>C (p.Leu91Pro)	OSTN-AS1, OSTN (L91P)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2304445	NM_198184.2(OSTN):c.245G>A (p.Arg82Lys)	OSTN, OSTN-AS1 (R82K)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 775208	NM_198184.2(OSTN):c.144A>G (p.Thr48=)	OSTN, OSTN-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign

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