ClinVar Miner

Submissions for variant NM_000231.2(SGCG):c.[800G>C;801T>C]

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000666684 SCV000791018 uncertain significance Autosomal recessive limb-girdle muscular dystrophy type 2C 2017-05-03 no assertion criteria provided clinical testing This submission and the accompanying classification are no longer maintained by the submitter. For more information on current observations and classification, please contact variantquestions@myriad.com.

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