ClinVar (all) for Orgtrack (Select 505471) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 199662	NM_000051.4(ATM):c.8732C>T (p.Thr2911Ile)	ATM, C11orf65 (T2911I)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 141183	NM_000051.4(ATM):c.2021A>G (p.His674Arg)	ATM (H674R)	Single nucleotide variant (missense variant)	Breast and/or ovarian cancer +5 more	GConflicting classifications of pathogenicity