List of variants in gene ACO2 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001098.3(ACO2):c.670C>T (p.Leu224=)	rs1799932	0.36650
NM_001098.3(ACO2):c.192A>C (p.Thr64=)	rs137831	0.29094
NM_001098.3(ACO2):c.220C>G (p.Leu74Val)	rs141772938	0.00383
NM_001098.3(ACO2):c.719G>C (p.Gly240Ala)	rs141878785	0.00064
NM_001098.3(ACO2):c.987C>T (p.Asp329=)	rs140823998	0.00029
NM_001098.3(ACO2):c.950A>G (p.Asn317Ser)	rs141739827	0.00021
NM_001098.3(ACO2):c.52C>T (p.Arg18Trp)	rs201569120	0.00018
NM_001098.3(ACO2):c.787G>T (p.Ala263Ser)	rs2066472274	0.00001
NM_001098.3(ACO2):c.91A>G (p.Lys31Glu)

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