ClinVar Miner

List of variants studied for Pierre Robin syndrome associated with collagen disease by Center for Human Genetics and Laboratory Diagnostics, Dr. Klein, Dr. Rost and Colleagues

Included ClinVar conditions (15):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP
NM_001844.4(COL2A1):c.609+4delA rs1555168965

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