List of variants in gene AK2 reported as uncertain significance for AK2-related disorder

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001625.4(AK2):c.422G>C (p.Gly141Ala)	rs541879563	0.00003
NM_001625.4(AK2):c.655G>A (p.Val219Met)	rs755736918	0.00003
NM_001625.4(AK2):c.470A>G (p.Asn157Ser)	rs371672441	0.00002
NM_001625.4(AK2):c.455A>G (p.Tyr152Cys)

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