ClinVar Miner

List of variants in gene combination CD99L2, GPR50, HMGB3, MAMLD1, MTM1, MTMR1, VMA21 reported as uncertain significance for X-linked myopathy with excessive autophagy

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency

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