ClinVar Miner

List of variants in gene GRXCR1 reported as benign for Autosomal recessive nonsyndromic hearing loss 25

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Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_001080476.3(GRXCR1):c.*55G>A rs4861050 0.45974
NM_001080476.3(GRXCR1):c.140C>T (p.Ala47Val) rs57655409 0.07551
NM_001080476.3(GRXCR1):c.272G>T (p.Gly91Val) rs113203706 0.00339
NM_001080476.3(GRXCR1):c.25G>A (p.Glu9Lys) rs78136490
NM_001080476.3(GRXCR1):c.627+8A>C rs10213360

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