Related gene-specific medical variations for Gene (Select 220965) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3091865	NM_198215.4(FAM13C):c.1671T>G (p.Asp557Glu)	FAM13C, PHYHIPL (D473E +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 980923	GRCh37/hg19 10q21.1(chr10:61110523-61179023)x1	FAM13C	Copy number loss	not provided	GLikely benign
Select item 815352	GRCh37/hg19 10q21.1-21.2(chr10:61110523-61203315)x1	FAM13C	Copy number loss	not provided	GLikely benign
Select item 161530	NM_198215.4(FAM13C):c.1427T>A (p.Leu476His)	FAM13C (L393H +7 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance

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