Related gene-specific medical variations for Gene (Select 80034) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3078385	NM_001172173.2(CSRNP3):c.40G>A (p.Gly14Ser)	CSRNP3, LOC129935044 (G14S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1340267	GRCh37/hg19 2q24.3(chr2:166322207-166374955)x1	CSRNP3	Copy number loss	not provided	GUncertain significance
Select item 687153	GRCh37/hg19 2q24.3(chr2:166352316-166433432)x3	CSRNP3	Copy number gain	not provided	GUncertain significance

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