ClinVar Miner

List of variants in gene LOC110806306, TERC studied for anemia (disease)

Included ClinVar conditions (264):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP
NR_001566.1(TERC):n.-240_-239del rs199422255
NR_001566.1(TERC):n.11G>T rs1159032173
NR_001566.1(TERC):n.18C>T
NR_001566.1(TERC):n.20T>C rs1060502987
NR_001566.1(TERC):n.28_34del rs199422259
NR_001566.1(TERC):n.29T>A rs1336050074
NR_001566.1(TERC):n.2G>C rs199422257
NR_001566.1(TERC):n.35C>T rs199422260
NR_001566.1(TERC):n.36C>T rs1248582778
NR_001566.1(TERC):n.37A>G rs199422261
NR_001566.1(TERC):n.37A>T
NR_001566.1(TERC):n.42_43dup rs1350357211
NR_001566.1(TERC):n.43T>G rs1553915624
NR_001566.1(TERC):n.48A>G rs199422262
NR_001566.1(TERC):n.53_87del rs199422264
NR_001566.1(TERC):n.54_57del rs199422263
NR_001566.1(TERC):n.58G>A rs113487931
NR_001566.1(TERC):n.66C>A
NR_001566.1(TERC):n.69_74dup rs1553915621
NR_001566.1(TERC):n.7C>A rs781517281

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