ClinVar Miner

List of variants in gene COL11A1 reported as uncertain significance by National Institute on Deafness and Communication Disorders, National Institutes of Health

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001854.4(COL11A1):c.1031C>T (p.Thr344Met)	rs544289862	0.00002
NM_001854.4(COL11A1):c.1314G>A (p.Met438Ile)	rs1666772918

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