ClinVar Miner

List of variants in gene COL9A1 reported as uncertain significance for Pierre Robin syndrome associated with collagen disease

Included ClinVar conditions (15):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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NM_001851.5(COL9A1):c.1634G>A (p.Arg545His) rs145698301
NM_001851.5(COL9A1):c.353G>A (p.Arg118Gln) rs143848379
NM_001851.5(COL9A1):c.626G>A (p.Arg209Lys) rs571441243

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