List of variants in gene combination FANCD2, FANCD2OS reported 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
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001018115.3(FANCD2):c.4281+115C>A	rs78896323	0.00165
NM_001018115.3(FANCD2):c.3466+10C>T	rs200208121	0.00034
NM_001018115.3(FANCD2):c.4281+37G>A	rs376442380	0.00008
NM_001018115.3(FANCD2):c.3290G>A (p.Arg1097Gln)	rs755748094	0.00006
NM_001018115.3(FANCD2):c.4281+107T>C	rs767893462	0.00004
NM_001018115.3(FANCD2):c.3523A>G (p.Ser1175Gly)	rs1267974483	0.00002
NM_001018115.3(FANCD2):c.3959A>G (p.His1320Arg)	rs746501818	0.00002
NM_001018115.3(FANCD2):c.3200A>G (p.Gln1067Arg)	rs771059153	0.00001
NM_001018115.3(FANCD2):c.3221C>A (p.Ala1074Asp)	rs772237103	0.00001
NM_001018115.3(FANCD2):c.3481C>T (p.Gln1161Ter)	rs369022159	0.00001
NM_001018115.3(FANCD2):c.3558C>G (p.Leu1186=)	rs745765337	0.00001
NM_001018115.3(FANCD2):c.4274C>A (p.Ala1425Asp)	rs1031002548	0.00001
NM_001018115.3(FANCD2):c.4281+69G>A	rs754606069	0.00001
NM_001018115.3(FANCD2):c.3163T>C (p.Tyr1055His)	rs1553613571
NM_001018115.3(FANCD2):c.3385C>T (p.Gln1129Ter)	rs2125072527

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