ClinVar Miner

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

Included ClinVar conditions (281):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 18
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HGVS dbSNP
NM_002454.3(MTRR):c.1020C>T (p.Cys340=) rs201348649
NM_002454.3(MTRR):c.144C>T (p.Thr48=) rs138612190
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.177C>G (p.Thr59=) rs142098262
NM_002454.3(MTRR):c.1819G>A (p.Val607Ile) rs114259126
NM_002454.3(MTRR):c.210C>G (p.Arg70=) rs41282641
NM_002454.3(MTRR):c.246G>C (p.Pro82=) rs149300444
NM_002454.3(MTRR):c.288C>T (p.Leu96=) rs35587995
NM_002454.3(MTRR):c.463A>C (p.Arg155=) rs556611332
NM_002454.3(MTRR):c.540G>A (p.Val180=) rs149037732
NM_002454.3(MTRR):c.769T>A (p.Ser257Thr) rs2303080
NM_002454.3(MTRR):c.828G>A (p.Val276=) rs115289458
NM_002454.3(MTRR):c.876C>T (p.Thr292=) rs144724549
NM_002454.3(MTRR):c.879T>C (p.Thr293=) rs773629167

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