Related gene-specific medical variations for Gene (Select 317772) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3103727	NM_175065.3(H2AC21):c.78C>G (p.Phe26Leu)	H2AC21, LOC129931379 (F26L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103726	NM_175065.3(H2AC21):c.38C>T (p.Ala13Val)	H2AC21, LOC129931379 (A13V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103724	NM_175065.3(H2AC21):c.146C>G (p.Pro49Arg)	H2AC21, LOC129931379 (P49R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2639151	NM_175065.3(H2AC21):c.69T>C (p.Gly23=)	H2AC21, LOC129931379	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2639150	NM_175065.3(H2AC21):c.132C>G (p.Val44=)	H2AC21, LOC129931379	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2639149	NM_175065.3(H2AC21):c.138A>C (p.Ala46=)	H2AC21, LOC129931379	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2553498	NM_175065.3(H2AC21):c.32C>T (p.Ala11Val)	H2AC21, LOC129931379 (A11V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533548	NM_175065.3(H2AC21):c.65C>T (p.Ala22Val)	H2AC21, LOC129931379 (A22V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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