List of variants in gene FANCD2 reported as likely pathogenic 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: 8

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HGVS	dbSNP	gnomAD frequency
NC_000003.11:g.(?_10068070)_(10070406_10074515)del
NC_000003.11:g.(?_10068070)_(10094182_10101977)del
NC_000003.11:g.(?_10084233)_(10085286_?)del
NC_000003.11:g.(?_10094051)_(10109021_?)dup
NM_001018115.3(FANCD2):c.3095del (p.Asn1032fs)	rs1559399574
NM_001018115.3(FANCD2):c.39dup (p.Glu14fs)	rs1575723664
NM_001018115.3(FANCD2):c.64+1_64+2del	rs777719596
NM_001018115.3(FANCD2):c.64+2T>G	rs2124961184

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