ClinVar Miner

Submissions for variant NM_000249.3(MLH1):c.62C>T (p.Ala21Val) (rs63750706)

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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
International Society for Gastrointestinal Hereditary Tumours (InSiGHT)	RCV000075787	SCV000106797	pathogenic	Lynch syndrome I	2015-11-24	reviewed by expert panel	research

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