List of variants in gene combination FANCD2, FANCD2OS reported as likely benign for Hereditary breast ovarian cancer syndrome

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001018115.3(FANCD2):c.3964-67A>G	rs34363202	0.01419
NM_001018115.3(FANCD2):c.3684-22G>A	rs115247173	0.00883
NM_001018115.3(FANCD2):c.3850-72G>A	rs374988769	0.00174
NM_001018115.3(FANCD2):c.4038+8G>A	rs190990145	0.00047
NM_001018115.3(FANCD2):c.3466+32T>G	rs766103472	0.00009
NM_001018115.3(FANCD2):c.3300G>A (p.Gln1100=)	rs2125069569
NM_001018115.3(FANCD2):c.3560+42dup	rs777197502
NM_001018115.3(FANCD2):c.3561-26G>A	rs2125077451

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