ClinVar Miner

List of variants in gene PHKG2 reported as likely benign for carbohydrate metabolism disease

Included ClinVar conditions (161):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP
NM_000294.3(PHKG2):c.1035A>G (p.Ser345=)
NM_000294.3(PHKG2):c.174A>T (p.Thr58=) rs56207641
NM_000294.3(PHKG2):c.360A>G (p.Thr120=) rs149163610
NM_000294.3(PHKG2):c.393G>A (p.Arg131=) rs55751949
NM_000294.3(PHKG2):c.864C>T (p.His288=)
NM_000294.3(PHKG2):c.96-10G>T rs74015042

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