ClinVar Miner

List of variants in gene combination EPC2, KIF5C, LOC126806366, LOC126806367, LOC129934887, LOC129934888, LOC129934889, LOC129934890, LOC129934891, LOC129934892, LOC129934893, LOC129934894, LOC129934895, LOC129934896, LOC132088759, MBD5, ORC4 reported as pathogenic for intellectual disability, autosomal dominant 1

Included ClinVar conditions (1):

Intellectual disability, autosomal dominant 1

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
NC_000002.10:g.148447496_149377297del

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