List of variants in gene combination CDAN1, LOC130056931 reported as uncertain significance 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_138477.4(CDAN1):c.256C>T (p.Pro86Ser)	rs543791953	0.00022
NM_138477.4(CDAN1):c.324C>T (p.Ser108=)	rs945794101	0.00004
NM_138477.4(CDAN1):c.392G>A (p.Arg131His)	rs1165157914	0.00001
NM_138477.4(CDAN1):c.255G>A (p.Arg85=)	rs886051159
NM_138477.4(CDAN1):c.257C>T (p.Pro86Leu)	rs1442095399
NM_138477.4(CDAN1):c.274G>C (p.Gly92Arg)	rs1051388342
NM_138477.4(CDAN1):c.278_279delinsAT (p.Ser93Asn)	rs2140513573
NM_138477.4(CDAN1):c.313G>A (p.Glu105Lys)
NM_138477.4(CDAN1):c.333C>T (p.Ala111=)	rs1320661924
NM_138477.4(CDAN1):c.463G>A (p.Gly155Ser)
NM_138477.4(CDAN1):c.494C>T (p.Thr165Met)

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