List of variants in gene combination HGSNAT, LOC130000316 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_152419.3(HGSNAT):c.63G>A (p.Ala21=)	rs549139396	0.00256
NM_152419.3(HGSNAT):c.6C>A (p.Ser2Arg)	rs535427008	0.00008
NM_152419.3(HGSNAT):c.10G>C (p.Ala4Pro)	rs1277900870	0.00004

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