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: rs3788266
rs3788266
0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50
CUI: C1852197
Disease: MAJOR AFFECTIVE DISORDER 1
MAJOR AFFECTIVE DISORDER 1
Mental Disorders 0.020 1.000 2 2007 2011
dbSNP: rs3788266
rs3788266
0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
Mental Disorders 0.020 1.000 2 2007 2011
dbSNP: rs3788266
rs3788266
0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50
CUI: C1839839
Disease: MAJOR AFFECTIVE DISORDER 2
MAJOR AFFECTIVE DISORDER 2
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Mental Disorders 0.020 1.000 2 2007 2011
dbSNP: rs3788266
rs3788266
0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50
CUI: C1970945
Disease: MAJOR AFFECTIVE DISORDER 6
MAJOR AFFECTIVE DISORDER 6
Mental Disorders 0.020 1.000 2 2007 2011
dbSNP: rs3788266
rs3788266
0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50
CUI: C1970943
Disease: MAJOR AFFECTIVE DISORDER 4
MAJOR AFFECTIVE DISORDER 4
Mental Disorders 0.020 1.000 2 2007 2011
dbSNP: rs1051169
rs1051169
0.851 0.200 21 46602317 synonymous variant C/A;G;T snv 0.65
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2020 2020
dbSNP: rs1051169
rs1051169
0.851 0.200 21 46602317 synonymous variant C/A;G;T snv 0.65
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1051169
rs1051169
0.851 0.200 21 46602317 synonymous variant C/A;G;T snv 0.65
CUI: C0027765
Disease: nervous system disorder
nervous system disorder
Nervous System Diseases 0.010 1.000 1 2020 2020
dbSNP: rs1051169
rs1051169
0.851 0.200 21 46602317 synonymous variant C/A;G;T snv 0.65
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs1051169
rs1051169
0.851 0.200 21 46602317 synonymous variant C/A;G;T snv 0.65
CUI: C0014060
Disease: Encephalitis, St. Louis
Encephalitis, St. Louis
Infections; Nervous System Diseases 0.010 1.000 1 2020 2020
dbSNP: rs11911834
rs11911834
0.882 0.080 21 46602608 5 prime UTR variant G/A;T snv
CUI: C0344315
Disease: Depressed mood
Depressed mood
Behavior and Behavior Mechanisms 0.010 1.000 1 2009 2009
dbSNP: rs11911834
rs11911834
0.882 0.080 21 46602608 5 prime UTR variant G/A;T snv
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
Mental Disorders 0.010 1.000 1 2009 2009
dbSNP: rs11911834
rs11911834
0.882 0.080 21 46602608 5 prime UTR variant G/A;T snv
CUI: C0221480
Disease: Recurrent depression
Recurrent depression
Mental Disorders 0.010 1.000 1 2009 2009
dbSNP: rs11911834
rs11911834
0.882 0.080 21 46602608 5 prime UTR variant G/A;T snv
CUI: C0011570
Disease: Mental Depression
Mental Depression
Behavior and Behavior Mechanisms 0.010 1.000 1 2009 2009
dbSNP: rs2300403
rs2300403
1.000 0.080 21 46601141 intron variant C/A;G;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2007 2007
dbSNP: rs2839357
rs2839357
1.000 0.040 21 46602974 intron variant A/G snv 9.4E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs3788266
rs3788266
0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
Neoplasms 0.010 1.000 1 2011 2011
dbSNP: rs3788266
rs3788266
0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
Neoplasms 0.010 1.000 1 2011 2011
dbSNP: rs3788266
rs3788266
0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50
CUI: C0280474
Disease: Childhood Glioblastoma
Childhood Glioblastoma
Neoplasms 0.010 1.000 1 2011 2011
dbSNP: rs3788266
rs3788266
0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50
CUI: C0278878
Disease: Adult Glioblastoma
Adult Glioblastoma
Neoplasms 0.010 1.000 1 2011 2011
dbSNP: rs3788266
rs3788266
0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma
Neoplasms; Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs3788266
rs3788266
0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma
Neoplasms 0.010 1.000 1 2011 2011
dbSNP: rs3788266
rs3788266
0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50
CUI: C4086165
Disease: Childhood Neuroblastoma
Childhood Neuroblastoma
Neoplasms 0.010 1.000 1 2011 2011
dbSNP: rs9722
rs9722
0.776 0.200 21 46599326 3 prime UTR variant G/A snv 0.16; 2.4E-05 0.21
CUI: C0011570
Disease: Mental Depression
Mental Depression
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: C0221480
Disease: Recurrent depression
Recurrent depression
Mental Disorders 0.010 1.000 1 2009 2009