Related gene-specific medical variations for Gene (Select 285671) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 814691	GRCh37/hg19 5q12.3(chr5:63636358-63779238)x1	RNF180	Copy number loss	not provided	GUncertain significance
Select item 563074	GRCh37/hg19 5q12.3(chr5:63263538-63618972)x1	RNF180	Copy number loss	not provided	GLikely benign
Select item 146649	GRCh38/hg38 5q12.3(chr5:64344867-64370545)x1	RNF180	Copy number loss	See cases	GBenign

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