List of variants in gene combination FANCD2, FANCD2OS reported as likely pathogenic by CeGaT Center for Human Genetics Tuebingen

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_001018115.3(FANCD2):c.3817C>T (p.Arg1273Ter)	rs745930696	0.00002
NM_001018115.3(FANCD2):c.3481C>T (p.Gln1161Ter)	rs369022159	0.00001
NM_001018115.3(FANCD2):c.3799del (p.Tyr1267fs)	rs775517107	0.00001
NM_001018115.3(FANCD2):c.3224+1G>T	rs1468320596

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