List of variants in gene combination AGPS, LOC129935172 reported as 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_003659.4(AGPS):c.147C>T (p.Pro49=)	rs34442536	0.01033
NM_003659.4(AGPS):c.35G>A (p.Gly12Asp)	rs557931141	0.00005

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