ClinVar Miner

Submissions for variant NM_178138.6(LHX3):c.112A>G (p.Ile38Val)

dbSNP: rs1341469393
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City RCV000723285 SCV000854674 uncertain significance Non-acquired combined pituitary hormone deficiency with spine abnormalities 2018-05-08 no assertion criteria provided clinical testing

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