List of variants in gene ALDOB reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 31

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HGVS	dbSNP	gnomAD frequency
NM_000035.3(ALDOB):c.-211T>A	rs12337537	0.09709
NM_000035.4(ALDOB):c.448G>C (p.Ala150Pro)	rs1800546	0.00319
NM_000035.4(ALDOB):c.156T>G (p.Thr52=)	rs149671008	0.00302
NM_000035.4(ALDOB):c.799+6G>A	rs141888548	0.00251
NM_000035.4(ALDOB):c.-10-17C>T	rs182858853	0.00172
NM_000035.4(ALDOB):c.543T>G (p.Asn181Lys)	rs35885472	0.00086
NM_000035.4(ALDOB):c.525C>T (p.Ala175=)	rs144196914	0.00058
NM_000035.4(ALDOB):c.619G>C (p.Glu207Gln)	rs3739721	0.00046
NM_000035.4(ALDOB):c.681C>T (p.Thr227=)	rs61757689	0.00032
NM_000035.4(ALDOB):c.524C>A (p.Ala175Asp)	rs76917243	0.00030
NM_000035.4(ALDOB):c.582T>C (p.Asp194=)	rs141988626	0.00018
NM_000035.4(ALDOB):c.178C>T (p.Arg60Ter)	rs118204429	0.00010
NM_000035.4(ALDOB):c.760G>A (p.Val254Ile)	rs776649110	0.00003
NM_000035.4(ALDOB):c.966G>A (p.Glu322=)	rs149166711	0.00002
NM_000035.4(ALDOB):c.1014G>A (p.Ala338=)	rs546735701	0.00001
NM_000035.4(ALDOB):c.1095G>C (p.Ter365Tyr)	rs900220679	0.00001
NM_000035.4(ALDOB):c.136A>T (p.Arg46Trp)	rs41281039	0.00001
NM_000035.4(ALDOB):c.222C>T (p.Ile74=)	rs754735910	0.00001
NM_000035.4(ALDOB):c.538C>A (p.Gln180Lys)	rs574635615	0.00001
NM_000035.4(ALDOB):c.*513G>A
NM_000035.4(ALDOB):c.1005C>G (p.Asn335Lys)	rs78340951
NM_000035.4(ALDOB):c.112+5G>A
NM_000035.4(ALDOB):c.113-1G>C	rs748663340
NM_000035.4(ALDOB):c.223G>A (p.Gly75Arg)
NM_000035.4(ALDOB):c.282C>T (p.Phe94=)	rs549682194
NM_000035.4(ALDOB):c.508G>A (p.Ala170Thr)
NM_000035.4(ALDOB):c.606C>T (p.Cys202=)
NM_000035.4(ALDOB):c.738A>G (p.Pro246=)	rs781139407
NM_000035.4(ALDOB):c.759C>A (p.Thr253=)	rs146360505
NM_000035.4(ALDOB):c.800-7C>T
NM_000035.4(ALDOB):c.921G>A (p.Gln307=)

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