ClinVar Miner

List of variants reported as uncertain significance for congenital muscular dystrophy due to integrin alpha-7 deficiency by Fulgent Genetics,Fulgent Genetics

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
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HGVS dbSNP
NM_002206.3(ITGA7):c.2035C>A (p.Leu679Met) rs142326016
NM_002206.3(ITGA7):c.2087C>T (p.Ser696Leu) rs76938320
NM_002206.3(ITGA7):c.2909C>T (p.Ala970Val) rs201354330
NM_002206.3(ITGA7):c.3203C>T (p.Ala1068Val) rs139136931

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