Related gene-specific medical variations for Gene (Select 493829) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3150184	NM_152901.4(PYDC1):c.233T>C (p.Met78Thr)	PYDC1, TRIM72 (M78T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3150183	NM_152901.4(PYDC1):c.223G>T (p.Asp75Tyr)	PYDC1, TRIM72 (D75Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3150182	NM_152901.4(PYDC1):c.191A>G (p.Tyr64Cys)	PYDC1, TRIM72 (Y64C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2484431	NM_152901.4(PYDC1):c.247G>C (p.Ala83Pro)	PYDC1, TRIM72 (A83P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2292720	NM_152901.4(PYDC1):c.161A>G (p.Asp54Gly)	PYDC1, TRIM72 (D54G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 157363	NC_000016.10:g.31209548_31215370del	TRIM72	Deletion	Small for gestational age	Gnot provided

ClinVar