List of variants in gene combination LOC129996933, OSTM1 reported as likely benign 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_014028.4(OSTM1):c.134A>G (p.Asp45Gly)	rs202093691	0.00068
NM_014028.4(OSTM1):c.49T>G (p.Trp17Gly)	rs546399681	0.00028

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