Related gene-specific medical variations for Gene (Select 10777) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 689176	GRCh37/hg19 3p22.3(chr3:35796715-35948815)x3	ARPP21	Copy number gain	not provided	GUncertain significance
Select item 687725	GRCh37/hg19 3p22.3(chr3:35796715-35948815)x3	ARPP21	Copy number gain	not provided	GUncertain significance
Select item 686431	GRCh37/hg19 3p22.3(chr3:35803643-35948815)x3	ARPP21	Copy number gain	not provided	GUncertain significance
Select item 221798	GRCh37/hg19 3p22.3(chr3:35832877-35925872)x3	ARPP21	Copy number gain	Premature ovarian failure	GBenign
Select item 161701	NM_001385562.1(ARPP21):c.1355G>T (p.Gly452Val)	ARPP21 (G452V +12 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance

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