ClinVar Miner

List of variants reported as uncertain significance for Pierre Robin syndrome associated with collagen disease by Mayo Clinic Genetic Testing Laboratories,Mayo Clinic

Included ClinVar conditions (15):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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HGVS dbSNP
NM_001844.5(COL2A1):c.2618G>T (p.Gly873Val) rs886042009
NM_001852.4(COL9A2):c.458C>T (p.Pro153Leu) rs77937237
NM_080679.2(COL11A2):c.628A>G (p.Ile210Val) rs778295133

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