ClinVar Miner

List of variants in gene combination NHP2, RMND5B reported as pathogenic for anemia (disease)

Included ClinVar conditions (263):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP
NM_022762.5(RMND5B):c.*1683A>T rs121908091
NM_022762.5(RMND5B):c.*1728A>G rs121908089
NM_022762.5(RMND5B):c.*1767C>T rs121908090

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