Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs35887622
rs35887622
GJB2
0.040 GeneticVariation BEFREE In addition, we found three patients with compound p.M34T mutation also exhibiting mild to moderate SNHI. 22668073

2012
dbSNP: rs35887622
rs35887622
GJB2
0.040 GeneticVariation BEFREE Patients with M34T mutations and/or mild SNHL had a low risk of progression. 19235794

2009
dbSNP: rs35887622
rs35887622
GJB2
0.040 GeneticVariation BEFREE Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing loss. 11134236

2001
dbSNP: rs35887622
rs35887622
GJB2
0.040 GeneticVariation BEFREE Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delT. 10903123

2000