ClinVar Miner

List of variants in gene combination ATM, C11orf65 reported as pathogenic for T-cell non-Hodgkin lymphoma

Included ClinVar conditions (3):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.7271T>G (p.Val2424Gly)	rs28904921	0.00006
NM_000051.4(ATM):c.7638_7646del (p.Arg2547_Ser2549del)	rs587776547

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