ClinVar for Gene (Select 101929529) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2312289	NM_001370181.1(GSTCD):c.1453A>G (p.Ser485Gly)	GSTCD, GSTCD-AS1 (S485G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247687	NM_001370181.1(GSTCD):c.1390C>T (p.Pro464Ser)	GSTCD, GSTCD-AS1 (P377S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 58034	GRCh38/hg38 4q24-25(chr4:105778347-110206873)x3	AIMP1, CASP6 +106 more	Copy number gain	See cases	GPathogenic
Select item 58033	GRCh38/hg38 4q22.3-28.3(chr4:96092893-136410207)x3	ABHD18, ADAD1 +661 more	Copy number gain	See cases	GPathogenic

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