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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_000035.4(ALDOB):c.*1151A>G	rs491979	0.46095
NM_000035.4(ALDOB):c.800-76T>C	rs506571	0.41593
NM_000035.4(ALDOB):c.*69C>T	rs4577	0.41145
NM_000035.4(ALDOB):c.540+84A>C	rs1929480	0.25349
NM_000035.4(ALDOB):c.*505C>A	rs17772845	0.07844
NM_000035.4(ALDOB):c.*897G>A	rs17772839	0.07843
NM_000035.4(ALDOB):c.*552T>A	rs41308902	0.07841
NM_000035.4(ALDOB):c.*612A>G	rs41296049	0.07833
NM_000035.4(ALDOB):c.*206C>A	rs17772869	0.07315
NM_000035.4(ALDOB):c.*122G>A	rs41310087	0.05383
NM_000035.4(ALDOB):c.-10-209A>G	rs113443424	0.03318
NM_000035.4(ALDOB):c.-214G>A	rs185972191	0.00678
NM_000035.4(ALDOB):c.156T>G (p.Thr52=)	rs149671008	0.00302
NM_000035.4(ALDOB):c.*189C>T	rs185986022	0.00287
NM_000035.4(ALDOB):c.799+6G>A	rs141888548	0.00251
NM_000035.4(ALDOB):c.*1003A>G	rs80292759	0.00174
NM_000035.4(ALDOB):c.906T>C (p.Tyr302=)	rs138866018	0.00151
NM_000035.4(ALDOB):c.324+8C>G	rs118168553	0.00103
NM_000035.4(ALDOB):c.543T>G (p.Asn181Lys)	rs35885472	0.00086
NM_000035.4(ALDOB):c.325-19T>G	rs200798661	0.00066
NM_000035.4(ALDOB):c.799+11C>T	rs182245025	0.00051
NM_000035.4(ALDOB):c.619G>C (p.Glu207Gln)	rs3739721	0.00046
NM_000035.4(ALDOB):c.-1C>T	rs560091436	0.00001
NM_000035.4(ALDOB):c.538C>A (p.Gln180Lys)	rs574635615	0.00001
NM_000035.4(ALDOB):c.400C>A (p.Arg134Ser)	rs10123355
NM_000035.4(ALDOB):c.759C>T (p.Thr253=)	rs146360505

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