ClinVar Miner

Submissions for variant NM_004787.4(SLIT2):c.2712A>T (p.Lys904Asn)

dbSNP: rs1008555507
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Yale Center for Mendelian Genomics, Yale University RCV000845121 SCV000987057 pathogenic Congenital anomaly of kidney and urinary tract 2015-05-31 no assertion criteria provided literature only

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