ClinVar Miner

List of variants in gene GRXCR2 studied for perceptual disorders

Included ClinVar conditions (765):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_001080516.2(GRXCR2):c.543A>C (p.Leu181Phe) rs2569006 0.68522
NM_001080516.2(GRXCR2):c.292G>T (p.Gly98Cys) rs141629319 0.00050
NM_001080516.2(GRXCR2):c.580G>A (p.Glu194Lys) rs367826984 0.00018
NM_001080516.2(GRXCR2):c.323C>T (p.Ala108Val) rs773457218 0.00001
NM_001080516.2(GRXCR2):c.247C>T (p.Gln83Ter)
NM_001080516.2(GRXCR2):c.714dup (p.Gly239fs) rs587777424

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