List of variants in gene UFSP2 reported as likely benign

Minimum submission review status:		Collection method:
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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_018359.5(UFSP2):c.932G>C (p.Cys311Ser)	rs75415917	0.01385
NM_018359.5(UFSP2):c.997G>A (p.Ala333Thr)	rs143266705	0.00048
NM_018359.5(UFSP2):c.1035C>T (p.Val345=)	rs375980105	0.00027
NM_018359.5(UFSP2):c.1026A>G (p.Ala342=)
NM_018359.5(UFSP2):c.876G>A (p.Gln292=)
NM_018359.5(UFSP2):c.893A>G (p.Asn298Ser)

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