ClinVar Miner

Submissions for variant NM_000125.4(ESR1):c.30T>C (p.Ser10=)

dbSNP: rs2077647
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001655332 SCV001867762 benign not provided 2018-08-17 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002501993 SCV002809655 benign Familial cancer of breast; Estrogen resistance syndrome; Myocardial infarction, susceptibility to; Migraine with or without aura, susceptibility to, 1 2022-04-19 criteria provided, single submitter clinical testing

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