List of variants in gene combination CDAN1, LOC130056931 reported as 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_138477.4(CDAN1):c.320A>T (p.Gln107Leu)	rs4265781	0.41423
NM_138477.4(CDAN1):c.477C>T (p.Pro159=)	rs7167392	0.26335
NM_138477.4(CDAN1):c.443C>T (p.Ala148Val)	rs73410959	0.06134
NM_138477.4(CDAN1):c.386G>A (p.Arg129His)	rs12441516	0.00155

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