List of variants in gene DNAI2 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_023036.6(DNAI2):c.1000A>G (p.Met334Val)	rs779742315	0.00006
NM_023036.6(DNAI2):c.115G>A (p.Glu39Lys)	rs148885547	0.00006
NM_023036.6(DNAI2):c.1327G>A (p.Asp443Asn)	rs368225621	0.00004
NM_023036.6(DNAI2):c.535G>T (p.Ala179Ser)	rs749303157	0.00004
NM_023036.6(DNAI2):c.317A>T (p.Tyr106Phe)	rs761389658	0.00003
NM_023036.6(DNAI2):c.589G>A (p.Asp197Asn)	rs761171314	0.00003
NM_023036.6(DNAI2):c.978A>T (p.Glu326Asp)	rs763193003	0.00001
NM_023036.6(DNAI2):c.1130C>T (p.Pro377Leu)	rs199726930
NM_023036.6(DNAI2):c.1153G>A (p.Asp385Asn)	rs567531807
NM_023036.6(DNAI2):c.1663A>G (p.Ile555Val)	rs146727740
NM_023036.6(DNAI2):c.787C>G (p.Arg263Gly)	rs137852998

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