List of variants in gene combination FANCD2, FANCD2OS reported as likely benign for Fanconi anemia complementation group D2

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_001018115.3(FANCD2):c.4281+270A>G	rs17032386	0.03356
NM_001018115.3(FANCD2):c.4281+115C>A	rs78896323	0.00179
NM_001018115.3(FANCD2):c.3560+20C>T	rs55804542	0.00162
NM_001018115.3(FANCD2):c.4038+8G>A	rs190990145	0.00047
NM_001018115.3(FANCD2):c.4206A>G (p.Gln1402=)	rs745841768	0.00015
NM_001018115.3(FANCD2):c.4281+81G>A	rs145889419	0.00011
NM_001018115.3(FANCD2):c.3165C>T (p.Tyr1055=)	rs375929975	0.00009
NM_001018115.3(FANCD2):c.3850-17G>T	rs369702202	0.00005
NM_001018115.3(FANCD2):c.3466+9C>G	rs33998487	0.00003
NM_001018115.3(FANCD2):c.3126C>T (p.His1042=)	rs552885346	0.00001
NM_001018115.3(FANCD2):c.3441T>C (p.Ala1147=)	rs533541893	0.00001
NM_001018115.3(FANCD2):c.3459A>G (p.Glu1153=)	rs570459552	0.00001
NM_001018115.3(FANCD2):c.3963+11A>G	rs945877549	0.00001

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