List of variants in gene combination FANCD2, LOC107303338 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: 9

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HGVS	dbSNP
NM_033084.5(FANCD2):c.1275C>T (p.Tyr425=)	rs764447374
NM_033084.5(FANCD2):c.1336C>G (p.Leu446Val)	rs34557223
NM_033084.5(FANCD2):c.1367T>G (p.Leu456Arg)	rs35782247
NM_033084.5(FANCD2):c.1634A>G (p.Asn545Ser)	rs145522204
NM_033084.5(FANCD2):c.2022-5C>T	rs4019784
NM_033084.5(FANCD2):c.2067C>T (p.Tyr689=)	rs763189891
NM_033084.5(FANCD2):c.2469A>G (p.Gln823=)	rs574054963
NM_033084.5(FANCD2):c.2484G>A (p.Lys828=)	rs55980657
NM_033084.5(FANCD2):c.2613A>C (p.Lys871Asn)	rs56041034

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