ClinVar Miner

Submissions for variant NM_205850.3(SLC24A5):c.503C>G (p.Ser168Ter) (rs977118193)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center of Medical Genetics,Central South University RCV000851387 SCV000902478 pathogenic Skin/hair/eye pigmentation, variation in, 4 2019-03-26 no assertion criteria provided clinical testing

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