ClinVar Miner

List of variants in gene combination CCDC189, PHKG2 reported as uncertain significance for carbohydrate metabolism disease

Included ClinVar conditions (161):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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HGVS dbSNP
NM_000294.3(PHKG2):c.*1135C>T rs371856479
NM_000294.3(PHKG2):c.*211C>T rs886051915
NM_000294.3(PHKG2):c.*2154G>A rs886051918
NM_000294.3(PHKG2):c.*2585G>A rs886051920
NM_000294.3(PHKG2):c.*3879A>G rs886051921
NM_000294.3(PHKG2):c.*3988T>C rs886051922
NM_000294.3(PHKG2):c.*546C>T rs768683366
NM_000294.3(PHKG2):c.*846A>G rs886051917

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