List of variants in gene SBDS reported as uncertain significance for anemia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_016038.4(SBDS):c.173T>C (p.Val58Ala)	rs747222022	0.00002
NM_016038.4(SBDS):c.523C>T (p.Arg175Trp)	rs774976459	0.00001
NM_016038.4(SBDS):c.40A>G (p.Asn14Asp)
NM_016038.4(SBDS):c.443A>G (p.Lys148Arg)

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