ClinVar Miner

List of variants in gene TERC studied for anemia (disease)

Included ClinVar conditions (258):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 61
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HGVS dbSNP
NR_001566.1(TERC):n.100T>A rs199422269
NR_001566.1(TERC):n.107G>T rs1553915617
NR_001566.1(TERC):n.107_108delGCinsAG rs199476393
NR_001566.1(TERC):n.110_113delGACT rs199422270
NR_001566.1(TERC):n.116C>T rs199422272
NR_001566.1(TERC):n.117A>C rs199422273
NR_001566.1(TERC):n.122_125delGCGG rs1553915612
NR_001566.1(TERC):n.132C>T
NR_001566.1(TERC):n.134C>G rs1306157402
NR_001566.1(TERC):n.140G>A rs1469879190
NR_001566.1(TERC):n.143G>A rs199422274
NR_001566.1(TERC):n.150A>G
NR_001566.1(TERC):n.164A>C rs750837239
NR_001566.1(TERC):n.178G>A rs199422275
NR_001566.1(TERC):n.180C>T rs199422276
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.204C>G rs199422277
NR_001566.1(TERC):n.205C>T
NR_001566.1(TERC):n.216_229delGGCGGGTCGCCTGC rs199422278
NR_001566.1(TERC):n.217G>C rs1553915599
NR_001566.1(TERC):n.219G>A
NR_001566.1(TERC):n.226C>T rs1367910897
NR_001566.1(TERC):n.228G>A rs141686314
NR_001566.1(TERC):n.231C>T rs906136164
NR_001566.1(TERC):n.232A>C rs878855313
NR_001566.1(TERC):n.245del rs1171775942
NR_001566.1(TERC):n.267C>T rs762111072
NR_001566.1(TERC):n.280G>C rs776511480
NR_001566.1(TERC):n.305G>A rs199422279
NR_001566.1(TERC):n.306T>G rs1553915591
NR_001566.1(TERC):n.321C>T rs747154095
NR_001566.1(TERC):n.322G>A rs199422280
NR_001566.1(TERC):n.323C>T rs199422281
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.366G>T
NR_001566.1(TERC):n.374_1194del821 rs1553915517
NR_001566.1(TERC):n.389C>T
NR_001566.1(TERC):n.391C>T
NR_001566.1(TERC):n.391_392delCC rs199422283
NR_001566.1(TERC):n.407_408delTCinsAA rs1553915580
NR_001566.1(TERC):n.408C>G rs199422284
NR_001566.1(TERC):n.410C>G rs199422286
NR_001566.1(TERC):n.415C>T rs762726864
NR_001566.1(TERC):n.443C>A rs1553915577
NR_001566.1(TERC):n.444A>G
NR_001566.1(TERC):n.450G>A rs199422287
NR_001566.1(TERC):n.451C>T rs1060502986
NR_001566.1(TERC):n.72C>G rs199422265
NR_001566.1(TERC):n.79delC rs199422266
NR_001566.1(TERC):n.96_97delCT rs199422267
NR_001566.1(TERC):n.98G>A rs199422268
TERC, 143G-A
TERC, 212C-G
TERC, 325G-T

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