ClinVar Miner

List of variants reported as benign for Marshall syndrome by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (6):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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.651+16A>G	rs116303092	0.01555
NM_001854.4(COL11A1):c.2611-4C>T	rs79505593	0.01381

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