Related gene-specific medical variations for Gene (Select 60401) - ClinVar - NCBI

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Links from Gene

Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1340689	GRCh37/hg19 Xq12(chrX:65734663-65943963)x3	EDA2R	Copy number gain	not provided	GLikely benign
Select item 1340082	GRCh37/hg19 Xq12(chrX:65699710-66031097)x0	EDA2R	Copy number loss	not provided	GUncertain significance
Select item 979823	GRCh37/hg19 Xq12(chrX:65734663-66698653)x3	EDA2R	Copy number gain	not provided	GLikely benign
Select item 689337	GRCh37/hg19 Xq12(chrX:65597135-65836640)x1	EDA2R	Copy number loss	not provided	GUncertain significance
Select item 687828	GRCh37/hg19 Xq12(chrX:65605983-65853863)x1	EDA2R	Copy number loss	not provided	GUncertain significance
Select item 685887	GRCh37/hg19 Xq12(chrX:65768300-65937194)x3	EDA2R	Copy number gain	not provided	GUncertain significance
Select item 684920	GRCh37/hg19 Xq12(chrX:65766523-65931826)x2	EDA2R	Copy number gain	not provided	GUncertain significance
Select item 684886	GRCh37/hg19 Xq12(chrX:65695229-66037575)x1	EDA2R	Copy number loss	not provided	GUncertain significance
Select item 564852	GRCh37/hg19 Xq12(chrX:65742087-65952960)x3	EDA2R	Copy number gain	not provided	GLikely benign
Select item 443736	GRCh37/hg19 Xq12(chrX:65652308-66075182)x1	EDA2R	Copy number loss	See cases	GUncertain significance
Select item 442615	GRCh37/hg19 Xq12(chrX:65590188-66268526)x3	EDA2R	Copy number gain	See cases	GUncertain significance
Select item 441974	GRCh37/hg19 Xq12(chrX:65699710-66037575)x1	EDA2R	Copy number loss	See cases	GUncertain significance
Select item 253725	GRCh37/hg19 Xq12(chrX:65813415-65987187)x0	EDA2R	Copy number loss	See cases	GUncertain significance