Related gene-specific medical variations for Gene (Select 8351) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2614817	NM_021065.3(H2AC7):c.67G>A (p.Gly23Arg)	H2AC7, H3C4 +1 more (G23R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2568770	NM_021065.3(H2AC7):c.80C>T (p.Pro27Leu)	H2AC7, H3C4 +1 more (P27L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2524791	NM_021065.3(H2AC7):c.74A>G (p.Gln25Arg)	H2AC7, H3C4 +1 more (Q25R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2517176	NM_021065.3(H2AC7):c.91G>A (p.Val31Ile)	H2AC7, H3C4 +1 more (V31I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

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