ClinVar Miner

List of variants reported as likely benign for Fanconi anemia, complementation group D2 by Illumina Clinical Services Laboratory,Illumina

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Total variants: 11
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HGVS dbSNP
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
NM_033084.5(FANCD2):c.3105+15C>T rs460965
NM_173472.2(FANCD2OS):c.43+5113T>C rs17032386
NM_173472.2(FANCD2OS):c.43+8916C>T rs190990145

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