ClinVar Miner

Submissions for variant NM_007297.4(BRCA1):c.300+17del (rs730881449)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000159862 SCV000209910 benign Familial cancer of breast 2013-11-11 criteria provided, single submitter clinical testing The variant is found in HEREDICANCER,BR-OV-HEREDIC panel(s).
Invitae RCV000534786 SCV000635971 benign not provided 2018-11-25 criteria provided, single submitter clinical testing
Color RCV000580276 SCV000683179 likely benign Hereditary cancer-predisposing syndrome 2015-07-17 criteria provided, single submitter clinical testing

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