List of variants in gene UFSP2 reported as pathogenic for bone development disease

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_018359.5(UFSP2):c.1277A>C (p.Asp426Ala)	rs1554022725
NM_018359.5(UFSP2):c.1283A>G (p.His428Arg)	rs2095515802
NM_018359.5(UFSP2):c.868T>C (p.Tyr290His)	rs796052130
NM_018359.5(UFSP2):c.905G>C (p.Cys302Ser)	rs2153279702

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