List of variants in gene AGT 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000029.4(AGT):c.1301C>T (p.Ala434Val)	rs61751076	0.00026
NM_000029.4(AGT):c.412G>T (p.Ala138Ser)	rs61762539	0.00021
NM_001384479.1(AGT):c.1027G>A	rs150452789	0.00019
NM_001384479.1(AGT):c.862C>T	rs61762530	0.00013
NM_001384479.1(AGT):c.31A>C	rs13306155	0.00010
NM_001384479.1(AGT):c.647A>C	rs568010875	0.00009
NM_001384479.1(AGT):c.13G>A (p.Gly5Ser)	rs377164467	0.00004
NM_001384479.1(AGT):c.380C>T (p.Pro127Leu)	rs1173238921	0.00002
NM_001384479.1(AGT):c.952G>C (p.Asp318His)	rs151194891	0.00002
NM_001384479.1(AGT):c.76C>T (p.Arg26Trp)	rs761670478	0.00001
NM_000029.4(AGT):c.951C>T (p.Gly317=)	rs771576624
NM_001384479.1(AGT):c.374T>C	rs1558288088

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