ClinVar Miner

List of variants in gene CDIN1 studied for anemia

Included ClinVar conditions (288):
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Gene type:
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Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_001321759.2(CDIN1):c.273+82C>T rs10220785 0.95448
NM_001321759.2(CDIN1):c.274-82T>A rs6495863 0.95445
NM_001321759.2(CDIN1):c.148-19G>T rs11073191 0.95366
NM_001321759.2(CDIN1):c.477-55G>A rs2381887 0.78569
NM_001321759.2(CDIN1):c.476+33T>C rs3743338 0.55611
NM_001321759.2(CDIN1):c.217C>G (p.Leu73Val) rs3784678 0.43599
NM_001321759.2(CDIN1):c.707A>G (p.Tyr236Cys) rs768744226 0.00002
NM_001321759.2(CDIN1):c.281A>C (p.Tyr94Ser) rs587777101 0.00001
NM_001321759.2(CDIN1):c.206A>G (p.Tyr69Cys)
NM_001321759.2(CDIN1):c.281A>G (p.Tyr94Cys) rs587777101
NM_001321759.2(CDIN1):c.298G>T (p.Ala100Ser)
NM_001321759.2(CDIN1):c.533T>A (p.Leu178Gln) rs587777100
NM_001321759.2(CDIN1):c.59C>G (p.Pro20Arg) rs1595696464
NM_001321759.2(CDIN1):c.620G>A (p.Gly207Glu)
NM_001321759.2(CDIN1):c.689A>C (p.His230Pro) rs1595503440
NM_001321759.2(CDIN1):c.812C>A (p.Thr271Lys)
NM_001321759.2(CDIN1):c.98C>T (p.Pro33Leu)

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