ClinVar Miner

List of variants reported as likely benign for congenital muscular dystrophy due to integrin alpha-7 deficiency by Invitae

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 9
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HGVS dbSNP
NM_002206.3(ITGA7):c.111C>T (p.Asp37=) rs1555166186
NM_002206.3(ITGA7):c.1506-10G>A rs370761565
NM_002206.3(ITGA7):c.1567+8C>T rs755842392
NM_002206.3(ITGA7):c.1671C>T (p.Ala557=) rs570999139
NM_002206.3(ITGA7):c.193C>A (p.Arg65=) rs17854602
NM_002206.3(ITGA7):c.2197-8del rs1555161122
NM_002206.3(ITGA7):c.3057+8G>A rs149798650
NM_002206.3(ITGA7):c.3058-5C>T rs1555158331
NM_002206.3(ITGA7):c.66G>A (p.Leu22=) rs137962065

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