List of variants in gene ANKRD37, UFSP2 studied for bone disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_018359.5(UFSP2):c.1333G>A (p.Gly445Arg)	rs756355545	0.00001
NM_018359.5(UFSP2):c.1376A>C (p.Asn459Thr)	rs2477666289

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