List of variants in gene INPPL1 reported as benign for opsismodysplasia

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001567.4(INPPL1):c.1091-25A>G	rs2276047	0.32600
NM_001567.4(INPPL1):c.987A>G (p.Ser329=)	rs2276048	0.27525
NM_001567.4(INPPL1):c.518+14C>G	rs56353029	0.03122
NM_001567.4(INPPL1):c.909G>C (p.Lys303Asn)	rs17847215	0.00985

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