ClinVar Miner

List of variants in gene TERC reported as uncertain significance for anemia (disease)

Included ClinVar conditions (263):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP
NR_001566.1(TERC):n.132C>T rs1160164639
NR_001566.1(TERC):n.134C>G rs1306157402
NR_001566.1(TERC):n.140G>A rs1469879190
NR_001566.1(TERC):n.142C>A
NR_001566.1(TERC):n.150A>G
NR_001566.1(TERC):n.153G>A
NR_001566.1(TERC):n.157A>T
NR_001566.1(TERC):n.160C>T
NR_001566.1(TERC):n.164A>C rs750837239
NR_001566.1(TERC):n.191C>T rs756967332
NR_001566.1(TERC):n.193G>A rs753227339
NR_001566.1(TERC):n.199C>T
NR_001566.1(TERC):n.202T>C rs1277188982
NR_001566.1(TERC):n.205C>T rs1192146620
NR_001566.1(TERC):n.209G>C
NR_001566.1(TERC):n.217G>C rs1553915599
NR_001566.1(TERC):n.219G>A rs1277657900
NR_001566.1(TERC):n.226C>T rs1367910897
NR_001566.1(TERC):n.231C>T rs906136164
NR_001566.1(TERC):n.232A>C rs878855313
NR_001566.1(TERC):n.233G>A
NR_001566.1(TERC):n.242C>T
NR_001566.1(TERC):n.245del rs1171775942
NR_001566.1(TERC):n.258C>T
NR_001566.1(TERC):n.265C>T
NR_001566.1(TERC):n.267C>T rs762111072
NR_001566.1(TERC):n.280G>C rs776511480
NR_001566.1(TERC):n.284C>T
NR_001566.1(TERC):n.321C>T rs747154095
NR_001566.1(TERC):n.343_348dup
NR_001566.1(TERC):n.344C>T rs374793413
NR_001566.1(TERC):n.351C>G
NR_001566.1(TERC):n.360C>G rs777348518
NR_001566.1(TERC):n.360C>T rs777348518
NR_001566.1(TERC):n.362G>T rs1553915587
NR_001566.1(TERC):n.363G>C
NR_001566.1(TERC):n.366G>T rs1560578577
NR_001566.1(TERC):n.389C>T
NR_001566.1(TERC):n.391C>T
NR_001566.1(TERC):n.395G>T
NR_001566.1(TERC):n.415C>T rs762726864
NR_001566.1(TERC):n.444A>G rs1560578539
NR_001566.1(TERC):n.450G>A rs199422287
NR_001566.1(TERC):n.451C>T rs1060502986
NR_001566.1(TERC):n.93G>C

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