List of variants in gene NT5C3A reported as likely benign for anemia

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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_001002010.5(NT5C3A):c.91T>C (p.Phe31Leu)	rs72555707	0.01571
NM_001002010.5(NT5C3A):c.139-9025G>T	rs149839373	0.00020
NM_001002010.5(NT5C3A):c.354+6C>A	rs572060959	0.00013
NM_001002010.5(NT5C3A):c.129C>A (p.Ile43=)
NM_001002010.5(NT5C3A):c.21G>A (p.Ala7=)
NM_001002010.5(NT5C3A):c.354+17A>G

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