ClinVar Miner

List of variants reported as 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: 5
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HGVS dbSNP
NM_002206.3(ITGA7):c.1008C>T (p.Asp336=) rs145114073
NM_002206.3(ITGA7):c.1965T>C (p.Cys655=) rs7971022
NM_002206.3(ITGA7):c.285G>T (p.Pro95=) rs17854601
NM_002206.3(ITGA7):c.3018C>G (p.Ser1006=) rs17117883
NM_002206.3(ITGA7):c.824G>A (p.Arg275His) rs74867235

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