Related gene-specific medical variations for Gene (Select 203238) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1809071	GRCh37/hg19 9p22.3(chr9:15823399-15947615)x1	CCDC171	Copy number loss	not provided	GUncertain significance
Select item 815239	GRCh37/hg19 9p22.3(chr9:15901665-15994736)x1	CCDC171	Copy number loss	not provided	GUncertain significance
Select item 161830	NM_173550.4(CCDC171):c.2404C>T (p.Arg802Trp)	CCDC171 (R802W +2 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance

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