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Links from MedGen

Items: 3

VariationLocationGene(s)Protein changeCondition(s)Clinical significance
(Last reviewed)
Review status
1.
TJP2Autosomal dominant nonsyndromic hearing loss 51Pathogenic
(Nov 24, 2019)
no assertion criteria provided
2.
TJP2Autosomal dominant nonsyndromic hearing loss 51Pathogenic
(Feb 19, 2016)
no assertion criteria provided
3.
GRCh37:
Chr9:71704982-71840362
GRCh38:
Chr9:69090066-69225446
TJP2, LOC124292588Autosomal dominant nonsyndromic hearing loss 51Pathogenic
(Feb 16, 2016)
no assertion criteria provided
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