List of variants reported as likely benign for Essential hypertension, genetic; Renal tubular dysgenesis of genetic origin by Fulgent Genetics, Fulgent Genetics

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000029.4(AGT):c.1116A>G (p.Leu372=)	rs7080	0.94659
NM_000685.5(AGTR1):c.*86A>C	rs5186	0.20976
NM_000029.4(AGT):c.410C>T (p.Thr137Met)	rs34829218	0.00316
NM_000029.4(AGT):c.912C>T (p.Asn304=)	rs61757178	0.00280
NM_001384479.1(AGT):c.1298C>T	rs61751077	0.00138
NM_000685.5(AGTR1):c.1017C>T (p.Tyr339=)	rs138545856	0.00031
NM_001384479.1(AGT):c.830-20G>A	rs371187328	0.00010
NM_000029.4(AGT):c.1395T>C (p.Tyr465=)	rs371051808	0.00006
NM_001384479.1(AGT):c.363G>A	rs752658346	0.00005
NM_001384479.1(AGT):c.264C>T (p.Thr88=)	rs11557884	0.00004
NM_001384479.1(AGT):c.282C>T	rs756049025	0.00003
NM_000029.4(AGT):c.396C>T (p.Thr132=)	rs201189192	0.00001
NM_001384479.1(AGT):c.906C>A	rs776504572

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