ClinVar Miner

List of variants in gene combination NHP2, RMND5B reported as uncertain significance 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
NC_000005.9:g.(?_177576708)_(177580824_?)del
NM_022762.5(RMND5B):c.*1748_*1755dup rs755460344
NM_022762.5(RMND5B):c.*1760A>G rs759145032

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