ClinVar Miner

List of variants in gene AGT reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 32
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HGVS dbSNP
NM_000029.3(AGT):c.-186G>A rs886046086
NM_000029.3(AGT):c.-191C>T rs886046087
NM_000029.3(AGT):c.-222G>A rs61762543
NM_000029.3(AGT):c.-298G>A rs5048
NM_000029.3(AGT):c.-320C>T rs61757165
NM_000029.3(AGT):c.-400T>C rs36218431
NM_000029.3(AGT):c.-423G>A rs5047
NM_000029.3(AGT):c.-48G>A rs886046085
NM_000029.4(AGT):c.*167T>C rs5043
NM_000029.4(AGT):c.*287G>A rs765914094
NM_000029.4(AGT):c.*384A>C rs886046079
NM_000029.4(AGT):c.*423T>G rs5044
NM_000029.4(AGT):c.*508C>T rs886046078
NM_000029.4(AGT):c.*513C>A rs886046077
NM_000029.4(AGT):c.*514G>A rs767078016
NM_000029.4(AGT):c.*83G>A rs886046080
NM_000029.4(AGT):c.-29C>T rs5052
NM_000029.4(AGT):c.1154T>C (p.Val385Ala) rs61731499
NM_000029.4(AGT):c.1222G>A (p.Glu408Lys) rs886046081
NM_000029.4(AGT):c.1325C>T (p.Ser442Phe) rs61751077
NM_000029.4(AGT):c.1345C>G (p.Pro449Ala) rs61751078
NM_000029.4(AGT):c.151T>C (p.Cys51Arg) rs61731497
NM_000029.4(AGT):c.263T>C (p.Leu88Pro) rs886046084
NM_000029.4(AGT):c.274G>A (p.Ala92Thr) rs886046083
NM_000029.4(AGT):c.327G>A (p.Leu109=) rs886046082
NM_000029.4(AGT):c.412G>T (p.Ala138Ser) rs61762539
NM_000029.4(AGT):c.674A>C (p.Gln225Pro) rs568010875
NM_000029.4(AGT):c.843C>T (p.Tyr281=) rs543740975
NM_000029.4(AGT):c.883G>T (p.Ala295Ser) rs377397992
NM_000029.4(AGT):c.886G>A (p.Glu296Lys) rs139685563
NM_000029.4(AGT):c.891C>T (p.Pro297=) rs748569303
NM_000029.4(AGT):c.951C>T (p.Gly317=) rs771576624

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