Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137852999
rs137852999
TMPRSS3
G 0.800 CausalMutation CLINVAR

dbSNP: rs137853000
rs137853000
TMPRSS3
A 0.800 CausalMutation CLINVAR

dbSNP: rs28939084
rs28939084
TMPRSS3
A 0.800 CausalMutation CLINVAR

dbSNP: rs387906915
rs387906915
TMPRSS3
C 0.800 CausalMutation CLINVAR

dbSNP: rs1060499811
rs1060499811
TMPRSS3
T 0.700 CausalMutation CLINVAR

dbSNP: rs1237955948
rs1237955948
TMPRSS3
A 0.700 CausalMutation CLINVAR

dbSNP: rs1333651774
rs1333651774
TMPRSS3
0.700 GeneticVariation UNIPROT

dbSNP: rs1429442821
rs1429442821
TMPRSS3
T 0.700 CausalMutation CLINVAR

dbSNP: rs147231991
rs147231991
TMPRSS3
T 0.700 GeneticVariation CLINVAR

dbSNP: rs56264519
rs56264519
TMPRSS3
T 0.700 GeneticVariation CLINVAR

dbSNP: rs773780151
rs773780151
TMPRSS3
0.700 GeneticVariation UNIPROT

dbSNP: rs137852999
rs137852999
TMPRSS3
0.800 GeneticVariation UNIPROT Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness. 11424922

2001
dbSNP: rs137852999
rs137852999
TMPRSS3
0.800 GeneticVariation UNIPROT Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness. 11462234

2001
dbSNP: rs137853000
rs137853000
TMPRSS3
0.800 GeneticVariation UNIPROT Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness. 11424922

2001
dbSNP: rs137853000
rs137853000
TMPRSS3
0.800 GeneticVariation UNIPROT Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness. 11462234

2001
dbSNP: rs28939084
rs28939084
TMPRSS3
0.800 GeneticVariation UNIPROT Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness. 11462234

2001
dbSNP: rs28939084
rs28939084
TMPRSS3
0.800 GeneticVariation UNIPROT Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness. 11424922

2001
dbSNP: rs387906915
rs387906915
TMPRSS3
0.800 GeneticVariation UNIPROT Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness. 11462234

2001
dbSNP: rs387906915
rs387906915
TMPRSS3
0.800 GeneticVariation UNIPROT Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness. 11424922

2001
dbSNP: rs137852999
rs137852999
TMPRSS3
0.800 GeneticVariation UNIPROT The transmembrane serine protease (TMPRSS3) mutated in deafness DFNB8/10 activates the epithelial sodium channel (ENaC) in vitro. 12393794

2002
dbSNP: rs137852999
rs137852999
TMPRSS3
0.800 GeneticVariation UNIPROT Mutations in the TMPRSS3 gene are a rare cause of childhood nonsyndromic deafness in Caucasian patients. 11907649

2002
dbSNP: rs137853000
rs137853000
TMPRSS3
0.800 GeneticVariation UNIPROT The transmembrane serine protease (TMPRSS3) mutated in deafness DFNB8/10 activates the epithelial sodium channel (ENaC) in vitro. 12393794

2002
dbSNP: rs137853000
rs137853000
TMPRSS3
0.800 GeneticVariation UNIPROT Mutations in the TMPRSS3 gene are a rare cause of childhood nonsyndromic deafness in Caucasian patients. 11907649

2002
dbSNP: rs28939084
rs28939084
TMPRSS3
0.800 GeneticVariation UNIPROT Mutations in the TMPRSS3 gene are a rare cause of childhood nonsyndromic deafness in Caucasian patients. 11907649

2002
dbSNP: rs28939084
rs28939084
TMPRSS3
0.800 GeneticVariation UNIPROT The transmembrane serine protease (TMPRSS3) mutated in deafness DFNB8/10 activates the epithelial sodium channel (ENaC) in vitro. 12393794

2002