Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2706
Gene Symbol: GJB2
GJB2 		0.450 CausalMutation phenotype CLINVAR
Entrez Id: 9381
Gene Symbol: OTOF
OTOF 		0.400 CausalMutation phenotype CLINVAR
Entrez Id: 23562
Gene Symbol: CLDN14
CLDN14 		0.400 CausalMutation phenotype CLINVAR
Entrez Id: 494513
Gene Symbol: PJVK
PJVK 		0.400 CausalMutation phenotype CLINVAR
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.300 CausalMutation phenotype CLINVAR
Entrez Id: 345895
Gene Symbol: RSPH4A
RSPH4A 		0.300 Biomarker phenotype GENOMICS_ENGLAND
Entrez Id: 64072
Gene Symbol: CDH23
CDH23 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 1187
Gene Symbol: CLCNKA
CLCNKA 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 7007
Gene Symbol: TECTA
TECTA 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 29899
Gene Symbol: GPSM2
GPSM2 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 117531
Gene Symbol: TMC1
TMC1 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 125336
Gene Symbol: LOXHD1
LOXHD1 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 25861
Gene Symbol: WHRN
WHRN 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 2059
Gene Symbol: EPS8
EPS8 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 374462
Gene Symbol: PTPRQ
PTPRQ 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 286002
Gene Symbol: SLC26A4-AS1
SLC26A4-AS1 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 340990
Gene Symbol: OTOG
OTOG 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 7399
Gene Symbol: USH2A
USH2A 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 124590
Gene Symbol: USH1G
USH1G 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 254268
Gene Symbol: AKNAD1
AKNAD1 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 286676
Gene Symbol: ILDR1
ILDR1 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 153562
Gene Symbol: MARVELD2
MARVELD2 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 389207
Gene Symbol: GRXCR1
GRXCR1 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 4286
Gene Symbol: MITF
MITF 		0.300 Biomarker phenotype CTD_human Apparent digenic inheritance of Waardenburg syndrome type 2 (WS2) and autosomal recessive ocular albinism (AROA). 9158138 1997