Related gene-specific medical variations for Gene (Select 152138) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3311868	NM_001083308.1(PYDC2):c.212C>T (p.Ala71Val)	PYDC2, PYDC2-AS1 (A71V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150185	NM_001083308.1(PYDC2):c.277G>A (p.Val93Met)	PYDC2, PYDC2-AS1 (V93M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272436	NM_001083308.1(PYDC2):c.59A>G (p.Gln20Arg)	PYDC2, PYDC2-AS1 (Q20R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249798	NM_001083308.1(PYDC2):c.72C>G (p.Ser24Arg)	PYDC2, PYDC2-AS1 (S24R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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