List of variants in gene ACER3 reported as uncertain significance by Ambry 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_018367.7(ACER3):c.185G>A (p.Arg62Gln)	rs755357196	0.00001
NM_018367.7(ACER3):c.122T>G (p.Leu41Arg)	rs2496316227
NM_018367.7(ACER3):c.125T>A (p.Ile42Asn)
NM_018367.7(ACER3):c.289A>T (p.Ile97Leu)	rs776323067
NM_018367.7(ACER3):c.35G>A (p.Gly12Asp)
NM_018367.7(ACER3):c.376G>A (p.Val126Ile)
NM_018367.7(ACER3):c.434A>G (p.His145Arg)
NM_018367.7(ACER3):c.493A>G (p.Thr165Ala)	rs2495941476
NM_018367.7(ACER3):c.74A>G (p.Tyr25Cys)	rs2496050994

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