List of variants in gene combination CPLANE1, LOC129389274 reported as uncertain significance for bone disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001384732.1(CPLANE1):c.4388C>T (p.Thr1463Ile)	rs202103224	0.00016
NM_001384732.1(CPLANE1):c.4322A>G (p.Lys1441Arg)	rs372201329	0.00013
NM_001384732.1(CPLANE1):c.4355C>T (p.Ser1452Phe)	rs138792462	0.00006
NM_001384732.1(CPLANE1):c.4427C>T (p.Thr1476Met)	rs1396140286	0.00003
NM_001384732.1(CPLANE1):c.4461T>G (p.Ser1487Arg)	rs1023003480	0.00001
NM_001384732.1(CPLANE1):c.4469A>G (p.Asn1490Ser)
NM_001384732.1(CPLANE1):c.4475A>T (p.Tyr1492Phe)	rs895907055

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