List of variants in gene combination GLB1, LOC129936434, TMPPE reported as likely pathogenic 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000404.3(GLB1):c.[276G>A];[75+5G>C]
NM_000404.4(GLB1):c.29dup (p.Leu11fs)
NM_000404.4(GLB1):c.3G>A (p.Met1Ile)	rs780109160
NM_000404.4(GLB1):c.47del (p.Leu16fs)
NM_000404.4(GLB1):c.65_75+1del	rs1382394474

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