ClinVar Miner

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

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Total variants: 33
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HGVS dbSNP
NM_001018115.3(FANCD2):c.1278+15C>T
NM_033084.5(FANCD2):c.-6G>C rs3732974
NM_033084.5(FANCD2):c.1122A>G (p.Val374=) rs34046352
NM_033084.5(FANCD2):c.1137G>T (p.Val379=) rs72492997
NM_033084.5(FANCD2):c.1170C>T (p.Ser390=) rs112887807
NM_033084.5(FANCD2):c.1179T>C (p.Thr393=) rs72492998
NM_033084.5(FANCD2):c.1214A>G (p.Asn405Ser) rs73126218
NM_033084.5(FANCD2):c.1275C>T (p.Tyr425=) rs764447374
NM_033084.5(FANCD2):c.1401G>A (p.Thr467=) rs12330369
NM_033084.5(FANCD2):c.1413+14T>C rs12330599
NM_033084.5(FANCD2):c.1413+3A>G rs62245508
NM_033084.5(FANCD2):c.1414-9C>T rs35557429
NM_033084.5(FANCD2):c.1509C>T (p.Asn503=) rs6785756
NM_033084.5(FANCD2):c.1868A>C (p.Gln623Pro) rs36070315
NM_033084.5(FANCD2):c.195G>C (p.Gln65His) rs36084488
NM_033084.5(FANCD2):c.205+9T>G rs34113138
NM_033084.5(FANCD2):c.2124T>C (p.Phe708=) rs9809716
NM_033084.5(FANCD2):c.2141C>T (p.Pro714Leu) rs3864017
NM_033084.5(FANCD2):c.2148C>G (p.Thr716=) rs55856815
NM_033084.5(FANCD2):c.2702G>T (p.Gly901Val) rs35495399
NM_033084.5(FANCD2):c.2712C>T (p.Asn904=) rs35594075
NM_033084.5(FANCD2):c.516A>G (p.Ile172Met) rs35173688
NM_033084.5(FANCD2):c.577A>G (p.Thr193Ala) rs34936017
NM_033084.5(FANCD2):c.64+12G>C rs9833228
NM_033084.5(FANCD2):c.983G>A (p.Arg328Gln) rs35625434
NM_173472.2(FANCD2OS):c.43+4698G>A rs11716842
NM_173472.2(FANCD2OS):c.43+4710C>T rs9862958
NM_173472.2(FANCD2OS):c.43+4817A>C rs3826
NM_173472.2(FANCD2OS):c.43+5186T>C rs7647987
NM_173472.2(FANCD2OS):c.43+5211C>T rs7626117
NM_173472.2(FANCD2OS):c.43+7813A>C rs2272125
NM_173472.2(FANCD2OS):c.44-10734T>C rs9811771
NM_173472.2(FANCD2OS):c.44-5713G>A rs147675860

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