ClinVar Miner

List of variants reported as likely pathogenic for Brody myopathy

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
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HGVS dbSNP
NC_000016.10:g.28902912G>A
NM_004320.5(ATP2A1):c.1184+1G>A rs551660089
NM_004320.5(ATP2A1):c.1764_1764+2delinsTGG
NM_004320.5(ATP2A1):c.325-2A>T rs1567479853

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