Source: INFERRED

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 9187
Gene Symbol: SLC24A1
SLC24A1 		solute carrier family 24 member 1 0.716 0.154 9.2E-05
CUI: C0339535
Disease: Night blindness, congenital stationary
Night blindness, congenital stationary 		disease 0.720 strong 1.000 0 0 2010 2016
Entrez Id: 9187
Gene Symbol: SLC24A1
SLC24A1 		solute carrier family 24 member 1 0.716 0.154 9.2E-05
CUI: C3151193
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1D
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1D 		disease 0.600 None 1.000 0 5 2010 2015
Entrez Id: 9187
Gene Symbol: SLC24A1
SLC24A1 		solute carrier family 24 member 1 0.716 0.154 9.2E-05
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		disease 0.110 None 1.000 0 2 2016 2016
Entrez Id: 9187
Gene Symbol: SLC24A1
SLC24A1 		solute carrier family 24 member 1 0.716 0.154 9.2E-05
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		phenotype 0.100 None 1.000 1 1 2012 2012
Entrez Id: 9187
Gene Symbol: SLC24A1
SLC24A1 		solute carrier family 24 member 1 0.716 0.154 9.2E-05
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		phenotype 0.100 None 1.000 1 5 2012 2012
Entrez Id: 9187
Gene Symbol: SLC24A1
SLC24A1 		solute carrier family 24 member 1 0.716 0.154 9.2E-05
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		phenotype 0.100 None 1.000 1 1 2018 2018
Entrez Id: 9187
Gene Symbol: SLC24A1
SLC24A1 		solute carrier family 24 member 1 0.716 0.154 9.2E-05
CUI: C4024756
Disease: Abnormality of macular pigmentation
Abnormality of macular pigmentation 		disease 0.100 None 0 0
Entrez Id: 9187
Gene Symbol: SLC24A1
SLC24A1 		solute carrier family 24 member 1 0.716 0.154 9.2E-05
CUI: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0 		phenotype 0.100 None 0 0
Entrez Id: 9187
Gene Symbol: SLC24A1
SLC24A1 		solute carrier family 24 member 1 0.716 0.154 9.2E-05
CUI: C1298695
Disease: Hypoplasia of optic disc
Hypoplasia of optic disc 		disease 0.100 None 0 0
Entrez Id: 9187
Gene Symbol: SLC24A1
SLC24A1 		solute carrier family 24 member 1 0.716 0.154 9.2E-05
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		disease 0.100 None 0 0
Entrez Id: 9187
Gene Symbol: SLC24A1
SLC24A1 		solute carrier family 24 member 1 0.716 0.154 9.2E-05
CUI: C0456909
Disease: Blindness
Blindness 		phenotype 0.100 None 0 0
Entrez Id: 9187
Gene Symbol: SLC24A1
SLC24A1 		solute carrier family 24 member 1 0.716 0.154 9.2E-05
CUI: C0271183
Disease: Severe myopia
Severe myopia 		disease 0.100 None 0 0
Entrez Id: 9187
Gene Symbol: SLC24A1
SLC24A1 		solute carrier family 24 member 1 0.716 0.154 9.2E-05
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity 		phenotype 0.100 None 0 0
Entrez Id: 9187
Gene Symbol: SLC24A1
SLC24A1 		solute carrier family 24 member 1 0.716 0.154 9.2E-05
CUI: C0038379
Disease: Strabismus
Strabismus 		disease 0.100 None 0 0
Entrez Id: 9187
Gene Symbol: SLC24A1
SLC24A1 		solute carrier family 24 member 1 0.716 0.154 9.2E-05
CUI: C0028738
Disease: Nystagmus
Nystagmus 		disease 0.100 None 0 0
Entrez Id: 9187
Gene Symbol: SLC24A1
SLC24A1 		solute carrier family 24 member 1 0.716 0.154 9.2E-05
CUI: C4554036
Disease: Nystagmus, CTCAE 5.0
Nystagmus, CTCAE 5.0 		phenotype 0.100 None 0 0