ClinVar Miner

Submissions for variant NM_017849.4(TMEM127):c.-18C>T

dbSNP: rs121908813
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Familial Cancer Clinic, Veneto Institute of Oncology RCV000114818 SCV000148713 likely pathogenic - adrenal pheochromocytoma Pheochromocytoma no assertion criteria provided not provided Converted during submission to Likely pathogenic.
Seelig Lab, University of Washington RCV000767316 SCV000897881 not provided not provided no assertion provided in vitro

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