ClinVar Miner

List of variants reported as likely pathogenic for anemia (disease) by Hemoglobin and Genome Lab,University of Campinas

Included ClinVar conditions (258):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP
NM_000096.3(CP):c.2756T>C (p.Leu919Pro) rs1135401784
NM_000096.3(CP):c.2879-1G>T rs386134141

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