ClinVar Miner

List of variants in gene JARID2 reported as likely pathogenic for developmental delay with variable intellectual disability and dysmorphic facies

Included ClinVar conditions (1):

Developmental delay with variable intellectual disability and dysmorphic facies

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_004973.4(JARID2):c.1945+1G>A

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