ClinVar Miner

Submissions for variant NM_006953.4(UPK3A):c.605G>A (p.Gly202Asp)

dbSNP: rs121918187
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000000923 SCV000021073 uncertain significance Congenital anomalies of kidney and urinary tract 1 2006-06-01 no assertion criteria provided literature only

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