List of variants in gene combination FANCD2, FANCD2OS reported as benign for hematologic disorder

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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001018115.3(FANCD2):c.4281+172G>A	rs7626117	0.35108
NM_001018115.3(FANCD2):c.4281+685C>T	rs11716842	0.30572
NM_001018115.3(FANCD2):c.3849+13A>G	rs9811771	0.25616
NM_001018115.3(FANCD2):c.4281+197A>G	rs7647987	0.24912
NM_001018115.3(FANCD2):c.4281+566T>G	rs3826	0.24892
NM_001018115.3(FANCD2):c.4098T>G (p.Leu1366=)	rs2272125	0.24889
NM_001018115.3(FANCD2):c.4185+33T>C	rs2272124	0.24884
NM_001018115.3(FANCD2):c.4281+673G>A	rs9862958	0.08846
NM_001018115.3(FANCD2):c.3560+20C>T	rs55804542	0.00162
NM_001018115.3(FANCD2):c.3446C>T (p.Ala1149Val)	rs147675860	0.00063
NM_001018115.3(FANCD2):c.4038+8G>A	rs190990145	0.00047
NM_001018115.3(FANCD2):c.3466+10C>T	rs200208121	0.00034
NM_001018115.3(FANCD2):c.4206A>G (p.Gln1402=)	rs745841768	0.00015
NM_001018115.3(FANCD2):c.3777+83_3777+86del	rs773716319

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