ClinVar Miner

Submissions for variant NM_152263.4(TPM3):c.272G>C (p.Arg91Pro)

dbSNP: rs199474713
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneReviews RCV000034942 SCV000058557 not provided Congenital myopathy with fiber type disproportion no assertion provided literature only
TPM3 homepage - Leiden Muscular Dystrophy pages RCV000128696 SCV000172336 not provided not provided no assertion provided not provided

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