List of variants in gene combination FANCD2, LOC107303338 reported as benign by Genetic Services Laboratory, University of Chicago

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001018115.3(FANCD2):c.1122A>G (p.Val374=)	rs34046352	0.19892
NM_001018115.3(FANCD2):c.2141C>T (p.Pro714Leu)	rs3864017	0.19295
NM_001018115.3(FANCD2):c.2484G>A (p.Lys828=)	rs55980657	0.00869
NM_001018115.3(FANCD2):c.195G>C (p.Gln65His)	rs36084488	0.00738
NM_001018115.3(FANCD2):c.1634A>G (p.Asn545Ser)	rs145522204	0.00460
NM_001018115.3(FANCD2):c.1156T>G (p.Phe386Val)	rs149125003	0.00450
NM_001018115.3(FANCD2):c.983G>A (p.Arg328Gln)	rs35625434	0.00124
NM_001018115.3(FANCD2):c.205+9T>G	rs34113138	0.00056
NM_001018115.3(FANCD2):c.1414-9C>T	rs35557429

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