Related gene-specific medical variations for Gene (Select 7551) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2540634	NM_145914.3(ZSCAN21):c.845G>C (p.Cys282Ser)	ZNF3, ZSCAN21 (C282S)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2516480	NM_145914.3(ZSCAN21):c.796G>A (p.Val266Ile)	ZNF3, ZSCAN21 (V266I)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GLikely benign
Select item 2411646	NM_145914.3(ZSCAN21):c.1013G>T (p.Gly338Val)	ZNF3, ZSCAN21 (G338V +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2393417	NM_145914.3(ZSCAN21):c.1247A>G (p.Tyr416Cys)	ZNF3, ZSCAN21 (I382V +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2389813	NM_145914.3(ZSCAN21):c.1055G>A (p.Arg352Lys)	ZNF3, ZSCAN21 (E318K +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2296447	NM_145914.3(ZSCAN21):c.865A>G (p.Ser289Gly)	ZNF3, ZSCAN21 (S289G)	Single nucleotide variant (3 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2250789	NM_145914.3(ZSCAN21):c.890G>C (p.Arg297Thr)	ZNF3, ZSCAN21 (E263Q +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance

ClinVar