ClinVar Miner

List of variants reported as likely pathogenic for X-linked myopathy with postural muscle atrophy by Invitae

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 8
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HGVS dbSNP gnomAD frequency
NC_000023.10:g.(?_135292010)_(135292184_?)del
NM_001159699.2(FHL1):c.205-1G>A rs2073859427
NM_001159699.2(FHL1):c.377_379+24del rs2148373814
NM_001159699.2(FHL1):c.380-2A>G rs2148375467
NM_001159699.2(FHL1):c.498C>G (p.Cys166Trp) rs145445372
NM_001159699.2(FHL1):c.506G>A (p.Cys169Tyr) rs122458145
NM_001159699.2(FHL1):c.50T>C (p.Met17Thr)
NM_001159699.2(FHL1):c.874T>A (p.Cys292Ser) rs1556639771

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