ClinVar Miner

List of variants studied for inclusion body myopathy with Paget disease of bone and frontotemporal dementia by Centogene AG - the Rare Disease Company

Included ClinVar conditions (9):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_007126.5(VCP):c.374G>A (p.Gly125Asp) rs1563980403

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