ClinVar Miner

List of variants in gene MTRR reported as benign for anemia (disease)

Included ClinVar conditions (262):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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HGVS dbSNP
NM_002454.3(MTRR):c.1464A>G (p.Val488=) rs35890938
NM_002454.3(MTRR):c.1468A>G (p.Thr490Ala) rs41283145
NM_002454.3(MTRR):c.1536C>T (p.Ser512=) rs34172797
NM_002454.3(MTRR):c.1653G>A (p.Pro551=) rs139206262
NM_002454.3(MTRR):c.1761T>C (p.Tyr587=) rs6874544
NM_002454.3(MTRR):c.210C>G (p.Arg70=) rs41282641
NM_002454.3(MTRR):c.769T>A (p.Ser257Thr) rs2303080
NM_002454.3(MTRR):c.828G>A (p.Val276=) rs115289458

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