Related gene-specific medical variations for Gene (Select 80760) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1809417	GRCh37/hg19 10p14(chr10:7588527-7648751)x1	ITIH5	Copy number loss	not provided	GUncertain significance
Select item 563711	GRCh37/hg19 10p14(chr10:7514582-7701527)x1	ITIH5	Copy number loss	not provided	GLikely benign
Select item 161774	NM_030569.7(ITIH5):c.2545G>T (p.Asp849Tyr)	ITIH5 (D849Y +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance

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