ClinVar Miner

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

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Total variants: 33
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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_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_000685.5(AGTR1):c.893A>G (p.Asn298Ser) rs368951368 0.00016
NM_001384479.1(AGT):c.862C>T rs61762530 0.00013
NM_000685.5(AGTR1):c.340G>A (p.Ala114Thr) rs140542820 0.00010
NM_001384479.1(AGT):c.31A>C rs13306155 0.00010
NM_001384479.1(AGT):c.830-20G>A rs371187328 0.00010
NM_000685.5(AGTR1):c.697C>A (p.Pro233Thr) rs151206107 0.00009
NM_001384479.1(AGT):c.647A>C rs568010875 0.00009
NM_000029.4(AGT):c.1395T>C (p.Tyr465=) rs371051808 0.00006
NM_001384479.1(AGT):c.829+1G>T rs747815674 0.00006
NM_001384479.1(AGT):c.363G>A rs752658346 0.00005
NM_001384479.1(AGT):c.13G>A (p.Gly5Ser) rs377164467 0.00004
NM_001384479.1(AGT):c.264C>T (p.Thr88=) rs11557884 0.00004
NM_001384479.1(AGT):c.282C>T rs756049025 0.00003
NM_000685.5(AGTR1):c.113T>C (p.Ile38Thr) rs751575775 0.00002
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_000029.4(AGT):c.396C>T (p.Thr132=) rs201189192 0.00001
NM_000685.5(AGTR1):c.1080A>G (p.Ter360Trp) rs778604981 0.00001
NM_001384479.1(AGT):c.1060C>T rs778806374 0.00001
NM_001384479.1(AGT):c.76C>T (p.Arg26Trp) rs761670478 0.00001
NM_000029.4(AGT):c.951C>T (p.Gly317=) rs771576624
NM_000685.5(AGTR1):c.925T>C (p.Phe309Leu) rs764229950
NM_001384479.1(AGT):c.374T>C rs1558288088
NM_001384479.1(AGT):c.906C>A rs776504572

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