ClinVar Miner

List of variants in gene combination FANCD2, LOC107303338 reported as likely benign for anemia (disease)

Included ClinVar conditions (263):
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Total variants: 34
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HGVS dbSNP
NM_033084.5(FANCD2):c.1130A>G (p.His377Arg) rs141141752
NM_033084.5(FANCD2):c.1134+10A>G rs758751922
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.1275C>T (p.Tyr425=) rs764447374
NM_033084.5(FANCD2):c.1311G>A (p.Ser437=) rs564577177
NM_033084.5(FANCD2):c.1367T>G (p.Leu456Arg) rs35782247
NM_033084.5(FANCD2):c.1414-9C>T rs35557429
NM_033084.5(FANCD2):c.1440T>C (p.His480=) rs375412395
NM_033084.5(FANCD2):c.1470T>C (p.Asp490=) rs567183176
NM_033084.5(FANCD2):c.1675A>G (p.Ile559Val) rs201408009
NM_033084.5(FANCD2):c.182C>T (p.Thr61Met) rs35110529
NM_033084.5(FANCD2):c.183G>A (p.Thr61=) rs771445756
NM_033084.5(FANCD2):c.1868A>C (p.Gln623Pro) rs36070315
NM_033084.5(FANCD2):c.1917C>A (p.Ile639=) rs151224882
NM_033084.5(FANCD2):c.2103G>T (p.Pro701=) rs139033444
NM_033084.5(FANCD2):c.2124T>C (p.Phe708=) rs9809716
NM_033084.5(FANCD2):c.2273G>C (p.Cys758Ser) rs540805431
NM_033084.5(FANCD2):c.2418T>G (p.Pro806=) rs61751577
NM_033084.5(FANCD2):c.2495-4T>G rs1553612428
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.2826G>C (p.Thr942=) rs200118565
NM_033084.5(FANCD2):c.311T>C (p.Ile104Thr) rs143936557
NM_033084.5(FANCD2):c.438+8T>G rs762114353
NM_033084.5(FANCD2):c.491+10G>A rs17032279
NM_033084.5(FANCD2):c.516A>G (p.Ile172Met) rs35173688
NM_033084.5(FANCD2):c.538C>T (p.Leu180=) rs373835427
NM_033084.5(FANCD2):c.577A>G (p.Thr193Ala) rs34936017
NM_033084.5(FANCD2):c.672C>T (p.His224=) rs371928644
NM_033084.5(FANCD2):c.78A>C (p.Gln26His) rs45510294
NM_033084.5(FANCD2):c.813G>A (p.Ser271=) rs773072936
NM_033084.5(FANCD2):c.864C>T (p.Ser288=) rs780547790
NM_033084.5(FANCD2):c.986C>G (p.Ala329Gly) rs116736407

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