List of variants in gene GRXCR1 reported as pathogenic for autosomal recessive nonsyndromic hearing loss 25

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001080476.3(GRXCR1):c.627+19A>T	rs201824235	0.00019
NM_001080476.3(GRXCR1):c.628-9C>A	rs606231120	0.00003
NM_001080476.3(GRXCR1):c.412C>T (p.Arg138Cys)	rs267606856	0.00001
NM_001080476.3(GRXCR1):c.457T>G (p.Phe153Val)	rs770874273	0.00001
NM_001080476.3(GRXCR1):c.469G>T (p.Glu157Ter)	rs774844858	0.00001
NM_001080476.3(GRXCR1):c.181C>T (p.Gln61Ter)
NM_001080476.3(GRXCR1):c.229C>T (p.Gln77Ter)	rs267606855
NM_001080476.3(GRXCR1):c.385-2A>G	rs771844359
NM_001080476.3(GRXCR1):c.550G>T (p.Glu184Ter)	rs2109775078
NM_001080476.3(GRXCR1):c.672del (p.Asp225fs)

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