Source: CLINVAR

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: 57688
Gene Symbol: ZSWIM6
ZSWIM6 		zinc finger SWIM-type containing 6 0.626 0.577 1.00
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		group 0.100 None 1.000 3 1 2014 2017
Entrez Id: 57688
Gene Symbol: ZSWIM6
ZSWIM6 		zinc finger SWIM-type containing 6 0.626 0.577 1.00
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		phenotype 0.100 None 1.000 3 1 2014 2017
Entrez Id: 57688
Gene Symbol: ZSWIM6
ZSWIM6 		zinc finger SWIM-type containing 6 0.626 0.577 1.00
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		disease 0.100 None 1.000 3 1 2014 2017
Entrez Id: 57688
Gene Symbol: ZSWIM6
ZSWIM6 		zinc finger SWIM-type containing 6 0.626 0.577 1.00
CUI: C1863616
Disease: ACROMELIC FRONTONASAL DYSOSTOSIS
ACROMELIC FRONTONASAL DYSOSTOSIS 		disease 0.740 None 1.000 2 1 2014 2017
Entrez Id: 57688
Gene Symbol: ZSWIM6
ZSWIM6 		zinc finger SWIM-type containing 6 0.626 0.577 1.00
CUI: C0036857
Disease: Severe intellectual disability
Severe intellectual disability 		disease 0.120 None 1.000 1 1 2017 2017
Entrez Id: 57688
Gene Symbol: ZSWIM6
ZSWIM6 		zinc finger SWIM-type containing 6 0.626 0.577 1.00
CUI: C4693405
Disease: NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES
NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES 		disease 0.400 strong 1.000 0 1 2014 2014
Entrez Id: 84083
Gene Symbol: ZRANB3
ZRANB3 		zinc finger RANBP2-type containing 3 0.780 0.577 4.2E-21
CUI: C0009691
Disease: Congenital cataract
Congenital cataract 		disease 0.100 None 0 1
Entrez Id: 84083
Gene Symbol: ZRANB3
ZRANB3 		zinc finger RANBP2-type containing 3 0.780 0.577 4.2E-21
CUI: C0266544
Disease: Microcornea
Microcornea 		disease 0.100 None 0 1
Entrez Id: 84083
Gene Symbol: ZRANB3
ZRANB3 		zinc finger RANBP2-type containing 3 0.780 0.577 4.2E-21
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum 		disease 0.100 None 0 1
Entrez Id: 84083
Gene Symbol: ZRANB3
ZRANB3 		zinc finger RANBP2-type containing 3 0.780 0.577 4.2E-21
CUI: C0423224
Disease: Sunken eyes
Sunken eyes 		phenotype 0.100 None 0 1
Entrez Id: 84083
Gene Symbol: ZRANB3
ZRANB3 		zinc finger RANBP2-type containing 3 0.780 0.577 4.2E-21
CUI: C1838625
Disease: Warburg Sjo Fledelius syndrome
Warburg Sjo Fledelius syndrome 		disease 0.110 None < 0.001 0 6 2013 2013
Entrez Id: 7784
Gene Symbol: ZP3
ZP3 		zona pellucida glycoprotein 3 0.805 0.115 2.9E-04
CUI: C1328577
Disease: Empty follicle syndrome
Empty follicle syndrome 		disease 0.100 None 1.000 1 1 2017 2017
Entrez Id: 7784
Gene Symbol: ZP3
ZP3 		zona pellucida glycoprotein 3 0.805 0.115 2.9E-04
CUI: C4540205
Disease: OOCYTE MATURATION DEFECT 3
OOCYTE MATURATION DEFECT 3 		disease 0.600 None 1.000 0 1 2017 2017
Entrez Id: 22917
Gene Symbol: ZP1
ZP1 		zona pellucida glycoprotein 1 0.890 1.9E-21
CUI: C4014291
Disease: OOCYTE MATURATION DEFECT 1
OOCYTE MATURATION DEFECT 1 		disease 0.600 None 1.000 0 1 2014 2014
Entrez Id: 9326
Gene Symbol: ZNHIT3
ZNHIT3 		zinc finger HIT-type containing 3 0.666 0.462 5.5E-07
CUI: C1850055
Disease: PEHO syndrome
PEHO syndrome 		disease 0.730 limited 1.000 0 1 2017 2020
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711 		zinc finger protein 711 0.691 0.423 0.98
CUI: C0026351
Disease: Moderate intellectual disability
Moderate intellectual disability 		disease 0.100 None 1.000 2 1 2009 2017
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711 		zinc finger protein 711 0.691 0.423 0.98
CUI: C2749020
Disease: Mental Retardation, X-Linked, Znf711-Related
Mental Retardation, X-Linked, Znf711-Related 		disease 0.600 strong 1.000 2 5 2009 2017
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711 		zinc finger protein 711 0.691 0.423 0.98
CUI: C3714796
Disease: Isolated somatotropin deficiency
Isolated somatotropin deficiency 		disease 0.100 None 1.000 2 1 2009 2017
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711 		zinc finger protein 711 0.691 0.423 0.98
CUI: C1843367
Disease: Poor school performance
Poor school performance 		phenotype 0.100 None 0 2
Entrez Id: 57592
Gene Symbol: ZNF687
ZNF687 		zinc finger protein 687 0.821 0.154 0.97
CUI: C4085250
Disease: PAGET DISEASE OF BONE 6
PAGET DISEASE OF BONE 6 		disease 0.400 None 1.000 0 2 2016 2016
Entrez Id: 84146
Gene Symbol: ZNF644
ZNF644 		zinc finger protein 644 0.821 0.192 1.00
CUI: C3279997
Disease: MYOPIA 21, AUTOSOMAL DOMINANT
MYOPIA 21, AUTOSOMAL DOMINANT 		disease 0.600 None 1.000 0 3 2011 2014
Entrez Id: 199692
Gene Symbol: ZNF627
ZNF627 		zinc finger protein 627 0.861 0.231 0.33
CUI: C1842763
Disease: SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION
SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION 		disease 0.100 None 1.000 1 10 2011 2011
Entrez Id: 284346
Gene Symbol: ZNF575
ZNF575 		zinc finger protein 575 1.000 0.192 0.11
CUI: C1865349
Disease: Ethylmalonic encephalopathy
Ethylmalonic encephalopathy 		disease 0.100 None 1.000 6 13 2004 2018
Entrez Id: 116115
Gene Symbol: ZNF526
ZNF526 		zinc finger protein 526 0.890 0.192 0.52
CUI: C1843367
Disease: Poor school performance
Poor school performance 		phenotype 0.100 None 0 1
Entrez Id: 116115
Gene Symbol: ZNF526
ZNF526 		zinc finger protein 526 0.890 0.192 0.52
CUI: C1956257
Disease: Pulmonary Stenosis
Pulmonary Stenosis 		disease 0.100 None 0 1