List of variants in gene combination ALDOA, LOC112694756 reported by Mayo Clinic Laboratories, Mayo Clinic

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001365304.2(LOC112694756):c.*1508+17G>T	rs2071390	0.13976
NM_001243177.4(ALDOA):c.1200C>T (p.Ser400=)	rs77290575	0.01088
NM_001243177.4(ALDOA):c.411A>G (p.Thr137=)	rs76767223	0.00362
NM_001243177.4(ALDOA):c.1201G>A (p.Gly401Ser)	rs138824667	0.00256
NM_001243177.4(ALDOA):c.679C>T (p.Arg227Cys)	rs374042346	0.00025
NM_001243177.4(ALDOA):c.898C>T (p.His300Tyr)	rs144693278	0.00016
NM_001243177.4(ALDOA):c.926C>T (p.Thr309Ile)	rs368207656	0.00007
NM_001243177.4(ALDOA):c.1129G>T (p.Ala377Ser)	rs148828956	0.00003
NM_001243177.4(ALDOA):c.910G>A (p.Ala304Thr)	rs886051893	0.00003
NM_001243177.4(ALDOA):c.996G>C (p.Glu332Asp)	rs565013143	0.00001
NM_001243177.4(ALDOA):c.1111AAG[1] (p.Lys372del)
NM_001243177.4(ALDOA):c.202A>G (p.Lys68Glu)
NM_001365304.2(LOC112694756):c.1050-24_1050-21dup	rs2151018355
NM_001365304.2(LOC112694756):c.*1509-4T>C	rs2151019768

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