ClinVar Miner

List of variants reported as likely benign for Melorheostosis; Noonan syndrome 1; Cardiofaciocutaneous syndrome 3 by Fulgent Genetics, Fulgent Genetics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_002755.4(MAP2K1):c.237C>T (p.Gly79=)	rs148656020	0.00024
NM_002755.4(MAP2K1):c.693+20T>C	rs753107656	0.00001
NM_002755.4(MAP2K1):c.291+14_291+20delinsTCTCACCAATCACCA	rs1064795401

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