ClinVar Miner

List of variants reported as pathogenic for opsismodysplasia by Revvity Omics, Revvity

Included ClinVar conditions (1):

Opsismodysplasia

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001567.4(INPPL1):c.2213-2A>C	rs1948918434
NM_001567.4(INPPL1):c.306C>G (p.Tyr102Ter)	rs779291537
NM_001567.4(INPPL1):c.3551_3552+1del	rs777012152

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