ClinVar Miner

Submissions for variant NM_001982.3(ERBB3):c.4009G>A (p.Ala1337Thr) (rs755855285)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor-Hopkins Center for Mendelian Genomics,Johns Hopkins University RCV000239667 SCV000298030 likely pathogenic Acute myeloid leukemia, M6 type criteria provided, single submitter research
OMIM RCV000239667 SCV000852036 risk factor Acute myeloid leukemia, M6 type 2018-11-09 no assertion criteria provided literature only

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