ClinVar Miner

Submissions for variant NM_001379110.1(SLC9A6):c.1072A>G (p.Thr358Ala)

dbSNP: rs2521314119
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center RCV003387657 SCV004099185 uncertain significance not provided 2023-09-28 criteria provided, single submitter clinical testing PM2, PP3

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