EBF3, EBF transcription factor 3, 253738

N. diseases: 124; N. variants: 15
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1131692261
rs1131692261 		1.000 10 129877778 missense variant C/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		0.700 1.000 8 2009 2017
dbSNP: rs779003155
rs779003155 		1.000 10 129877779 missense variant G/A;T snv 4.0E-06
CUI: C4310618
Disease: HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME
HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME 		0.800 1.000 3 2017 2017
dbSNP: rs869312668
rs869312668 		1.000 10 129957282 missense variant G/A snv
CUI: C4310618
Disease: HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME
HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME 		0.800 1.000 3 2017 2017
dbSNP: rs1057519389
rs1057519389 		0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C4025865
Disease: Abnormality of facial musculature
Abnormality of facial musculature 		0.700 1.000 1 2017 2017
dbSNP: rs1057519389
rs1057519389 		0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C1848673
Disease: Hypoplastic feet
Hypoplastic feet 		0.700 1.000 1 2017 2017
dbSNP: rs1057519389
rs1057519389 		0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C1850049
Disease: Clinodactyly of the 5th finger
Clinodactyly of the 5th finger 		0.700 1.000 1 2017 2017
dbSNP: rs1057519389
rs1057519389 		0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		0.700 1.000 1 2017 2017
dbSNP: rs1057519389
rs1057519389 		0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C1837522
Disease: Impaired pain sensation
Impaired pain sensation 		0.700 1.000 1 2017 2017
dbSNP: rs1057519389
rs1057519389 		0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C1843367
Disease: Poor school performance
Poor school performance 		0.700 1.000 1 2017 2017
dbSNP: rs1057519389
rs1057519389 		0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C0566899
Disease: Small labia majora
Small labia majora 		0.700 1.000 1 2017 2017
dbSNP: rs1057519389
rs1057519389 		0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C1855676
Disease: Aplasia/Hypoplasia of the cerebellar vermis
Aplasia/Hypoplasia of the cerebellar vermis 		0.700 1.000 1 2017 2017
dbSNP: rs1057519389
rs1057519389 		0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C1865304
Disease: Overfolding of the superior helices
Overfolding of the superior helices 		0.700 1.000 1 2017 2017
dbSNP: rs1057519389
rs1057519389 		0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C1835884
Disease: Triangular face
Triangular face 		0.700 1.000 1 2017 2017
dbSNP: rs1057519389
rs1057519389 		0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C0454641
Disease: Expressive language delay
Expressive language delay 		0.700 1.000 1 2017 2017
dbSNP: rs1057519389
rs1057519389 		0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C0221358
Disease: Long narrow head
Long narrow head 		0.700 0
dbSNP: rs1057519389
rs1057519389 		0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C1844820
Disease: Range of joint movement increased
Range of joint movement increased 		0.700 0
dbSNP: rs1057519389
rs1057519389 		0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C1697450
Disease: obsolete Prominent epicanthal folds
obsolete Prominent epicanthal folds 		0.700 0
dbSNP: rs1057519389
rs1057519389 		0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C0234860
Disease: Weak cry
Weak cry 		0.700 0
dbSNP: rs1057519389
rs1057519389 		0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C1866195
Disease: Downturned corners of mouth
Downturned corners of mouth 		0.700 0
dbSNP: rs1057519389
rs1057519389 		0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C1837731
Disease: Overfolded helix
Overfolded helix 		0.700 0
dbSNP: rs1057519389
rs1057519389 		0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C4310618
Disease: HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME
HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME 		0.800 0
dbSNP: rs1057519389
rs1057519389 		0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C1865014
Disease: Long philtrum
Long philtrum 		0.700 0
dbSNP: rs1057519389
rs1057519389 		0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C4551492
Disease: Micropenis
Micropenis 		0.700 0
dbSNP: rs1057519389
rs1057519389 		0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C3278923
Disease: Dilated ventricles (finding)
Dilated ventricles (finding) 		0.700 0
dbSNP: rs1057519389
rs1057519389 		0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C1855333
Disease: External genital hypoplasia
External genital hypoplasia 		0.700 0