ClinVar Miner

List of variants in gene GRXCR1 reported as uncertain significance for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
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HGVS dbSNP
NM_001080476.2(GRXCR1):c.*69T>A rs796495255
NM_001080476.2(GRXCR1):c.*89G>A rs564643132
NM_001080476.2(GRXCR1):c.236G>A (p.Ser79Asn) rs886059416
NM_001080476.2(GRXCR1):c.284G>C (p.Arg95Thr) rs775363257
NM_001080476.2(GRXCR1):c.289G>A (p.Val97Ile) rs186041671
NM_001080476.2(GRXCR1):c.331T>C (p.Tyr111His) rs201002003
NM_001080476.2(GRXCR1):c.358T>C (p.Phe120Leu) rs529420082
NM_001080476.2(GRXCR1):c.385-7C>T rs748066741
NM_001080476.2(GRXCR1):c.439C>T (p.Arg147Cys) rs569193097
NM_001080476.2(GRXCR1):c.49C>T (p.Arg17Trp) rs762049276
NM_001080476.2(GRXCR1):c.551A>T (p.Glu184Val) rs886059417
NM_001080476.2(GRXCR1):c.604T>C (p.Phe202Leu) rs886059418
NM_001080476.2(GRXCR1):c.745C>G (p.Pro249Ala) rs886059419
NM_001080476.2(GRXCR1):c.785G>A (p.Arg262Gln) rs146696590
NM_001080476.2(GRXCR1):c.858G>T (p.Lys286Asn) rs886059420
NM_001080476.3(GRXCR1):c.*65A>G
NM_001080476.3(GRXCR1):c.*6G>T
NM_001080476.3(GRXCR1):c.325G>A (p.Val109Ile)

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