ClinVar Miner

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

Included ClinVar conditions (161):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP
NM_000035.4(ALDOB):c.*1003A>G rs80292759
NM_000035.4(ALDOB):c.*1151A>G rs491979
NM_000035.4(ALDOB):c.*122G>A rs41310087
NM_000035.4(ALDOB):c.*189C>T
NM_000035.4(ALDOB):c.*206C>A rs17772869
NM_000035.4(ALDOB):c.*505C>A rs17772845
NM_000035.4(ALDOB):c.*552T>A rs41308902
NM_000035.4(ALDOB):c.*612A>G rs41296049
NM_000035.4(ALDOB):c.*69C>T rs4577
NM_000035.4(ALDOB):c.*897G>A rs17772839
NM_000035.4(ALDOB):c.-1C>T rs560091436
NM_000035.4(ALDOB):c.-214G>A rs185972191
NM_000035.4(ALDOB):c.156T>G (p.Thr52=) rs149671008
NM_000035.4(ALDOB):c.324+8C>G rs118168553
NM_000035.4(ALDOB):c.400C>A (p.Arg134Ser) rs10123355
NM_000035.4(ALDOB):c.538C>A (p.Gln180Lys) rs574635615
NM_000035.4(ALDOB):c.543T>G (p.Asn181Lys) rs35885472
NM_000035.4(ALDOB):c.619G>C (p.Glu207Gln) rs3739721
NM_000035.4(ALDOB):c.759C>T (p.Thr253=) rs146360505
NM_000035.4(ALDOB):c.906T>C (p.Tyr302=) rs138866018

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