ClinVar Miner

List of variants in gene combination ATM, C11orf65, LOC128772356, LOC129390354 reported as uncertain significance for ataxia telangiectasia

Included ClinVar conditions (6):

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: 3

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HGVS	dbSNP	gnomAD frequency
NC_000011.9:g.(?_108115509)_(108236241_?)dup
NC_000011.9:g.(?_108126936)_(108236241_?)dup
NC_000011.9:g.(?_108137888)_(108236245_?)dup

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