S100B, S100 calcium binding protein B, 6285

N. diseases: 599; N. variants: 6
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: rs9722
rs9722 		0.776 0.200 21 46599326 3 prime UTR variant G/A snv 0.16; 2.4E-05 0.21
CUI: C0344315
Disease: Depressed mood
Depressed mood 		Behavior and Behavior Mechanisms 0.010 1.000 1 2009 2009
dbSNP: rs9722
rs9722 		0.776 0.200 21 46599326 3 prime UTR variant G/A snv 0.16; 2.4E-05 0.21
CUI: C0018572
Disease: Hand, Foot and Mouth Disease
Hand, Foot and Mouth Disease 		Infections 0.010 1.000 1 2019 2019
dbSNP: rs9722
rs9722 		0.776 0.200 21 46599326 3 prime UTR variant G/A snv 0.16; 2.4E-05 0.21
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		Mental Disorders 0.010 1.000 1 2009 2009
dbSNP: rs9722
rs9722 		0.776 0.200 21 46599326 3 prime UTR variant G/A snv 0.16; 2.4E-05 0.21
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression 		Mental Disorders 0.010 1.000 1 2008 2008
dbSNP: rs9722
rs9722 		0.776 0.200 21 46599326 3 prime UTR variant G/A snv 0.16; 2.4E-05 0.21
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs9722
rs9722 		0.776 0.200 21 46599326 3 prime UTR variant G/A snv 0.16; 2.4E-05 0.21
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.010 < 0.001 1 2008 2008
dbSNP: rs9722
rs9722 		0.776 0.200 21 46599326 3 prime UTR variant G/A snv 0.16; 2.4E-05 0.21
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2018 2018