Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1625579
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.900 0.893 26 2011 2019
dbSNP: rs1625579
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.720 1.000 2 2012 2013
dbSNP: rs2660304
rs2660304
MIR137HG ; MIR137 ; MIR2682
0.925 0.120 1 98046571 non coding transcript exon variant G/T snv 0.83
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.710 1.000 1 2015 2018
dbSNP: rs1625579
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78
CUI: C0349204
Disease: Nonorganic psychosis
Nonorganic psychosis 		0.020 1.000 2 2013 2014
dbSNP: rs1625579
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders 		0.020 1.000 2 2013 2014
dbSNP: rs1625579
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78
CUI: C0001726
Disease: Affective Symptoms
Affective Symptoms 		0.010 1.000 1 2014 2014
dbSNP: rs1625579
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78
CUI: C0871189
Disease: Psychotic symptom
Psychotic symptom 		0.010 1.000 1 2015 2015
dbSNP: rs1625579
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.010 1.000 1 2014 2014
dbSNP: rs1625579
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
Mucocutaneous Lymph Node Syndrome 		0.010 1.000 1 2018 2018
dbSNP: rs1625579
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes 		0.010 1.000 1 2018 2018
dbSNP: rs1625579
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78
CUI: C0036337
Disease: Schizoaffective Disorder
Schizoaffective Disorder 		0.010 1.000 1 2013 2013
dbSNP: rs1625579
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.010 1.000 1 2019 2019
dbSNP: rs2660304
rs2660304
MIR137HG ; MIR137 ; MIR2682
0.925 0.120 1 98046571 non coding transcript exon variant G/T snv 0.83
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.010 1.000 1 2019 2019