List of variants in gene NDUFS2 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001377299.1(NDUFS2):c.1290C>T (p.Ala430=)	rs1136207	0.11971
NM_001377299.1(NDUFS2):c.1054C>G (p.Pro352Ala)	rs11576415	0.06514
NM_001377299.1(NDUFS2):c.1138C>G (p.His380Asp)	rs144411579	0.00055
NM_001377299.1(NDUFS2):c.1276G>T (p.Ala426Ser)	rs186476170	0.00044
NM_001377299.1(NDUFS2):c.1324C>T (p.His442Tyr)	rs201897431	0.00005

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