ClinVar Miner

List of variants studied for COG6-congenital disorder of glycosylation by Centogene AG - the Rare Disease Company

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_020751.3(COG6):c.1167-24A>G rs730882236

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