Source: GWASCAT

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: rs35909029
rs35909029
LINC02210-CRHR1
1.000 0.040 17 45774132 intron variant T/A;C;G snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs35909029
rs35909029
LINC02210-CRHR1
1.000 0.040 17 45774132 intron variant T/A;C;G snv
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs365825
rs365825
LINC02210 ; LINC02210-CRHR1
1.000 0.040 17 45628235 intron variant A/G snv 0.29
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2016 2016
dbSNP: rs3843738
rs3843738
LINC02210-CRHR1 ; LOC105371802
17 45661828 intron variant A/G snv 0.37
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs393152
rs393152
LINC02210 ; LINC02210-CRHR1
0.851 0.160 17 45641777 non coding transcript exon variant A/G snv 0.18 0.29
CUI: C0393570
Disease: Corticobasal degeneration
Corticobasal degeneration 		0.700 1.000 1 2015 2015
dbSNP: rs393152
rs393152
LINC02210 ; LINC02210-CRHR1
0.851 0.160 17 45641777 non coding transcript exon variant A/G snv 0.18 0.29
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.810 1.000 1 2009 2015
dbSNP: rs4327090
rs4327090
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
17 45825175 intron variant A/G snv 0.12
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs62057061
rs62057061
LINC02210-CRHR1
1.000 0.040 17 45779273 intron variant C/G snv 0.14
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs62057061
rs62057061
LINC02210-CRHR1
1.000 0.040 17 45779273 intron variant C/G snv 0.14
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs62057107
rs62057107
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
17 45818666 intron variant C/G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs675600
rs675600
LINC02210 ; LINC02210-CRHR1
17 45618793 upstream gene variant A/T snv 0.14
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs675600
rs675600
LINC02210 ; LINC02210-CRHR1
17 45618793 upstream gene variant A/T snv 0.14
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs675600
rs675600
LINC02210 ; LINC02210-CRHR1
17 45618793 upstream gene variant A/T snv 0.14
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs675600
rs675600
LINC02210 ; LINC02210-CRHR1
17 45618793 upstream gene variant A/T snv 0.14
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs7207400
rs7207400
LINC02210-CRHR1
1.000 0.040 17 45746994 intron variant T/C snv 0.32
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7207400
rs7207400
LINC02210-CRHR1
1.000 0.040 17 45746994 intron variant T/C snv 0.32
CUI: C0003467
Disease: Anxiety
Anxiety 		0.700 1.000 1 2018 2018
dbSNP: rs7220839
rs7220839
LINC02210-CRHR1
1.000 0.040 17 45737779 intron variant C/T snv 0.47
CUI: C0003467
Disease: Anxiety
Anxiety 		0.700 1.000 1 2018 2018
dbSNP: rs7225384
rs7225384
LINC02210-CRHR1 ; LOC107985028
1.000 0.040 17 45731730 non coding transcript exon variant C/G snv 0.39
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs7225384
rs7225384
LINC02210-CRHR1 ; LOC107985028
1.000 0.040 17 45731730 non coding transcript exon variant C/G snv 0.39
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs77804065
rs77804065
LINC02210-CRHR1 ; LOC107985028
17 45733530 splice region variant C/A;G;T snv
CUI: C0018681
Disease: Headache
Headache 		0.700 1.000 1 2018 2018
dbSNP: rs9303521
rs9303521
LINC02210-CRHR1
0.925 0.120 17 45727828 intron variant T/C;G snv 0.60
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs9303521
rs9303521
LINC02210-CRHR1
0.925 0.120 17 45727828 intron variant T/C;G snv 0.60
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs9303521
rs9303521
LINC02210-CRHR1
0.925 0.120 17 45727828 intron variant T/C;G snv 0.60
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs9303521
rs9303521
LINC02210-CRHR1
0.925 0.120 17 45727828 intron variant T/C;G snv 0.60
CUI: C0037019
Disease: Shy-Drager Syndrome
Shy-Drager Syndrome 		0.700 1.000 1 2016 2016
dbSNP: rs9303521
rs9303521
LINC02210-CRHR1
0.925 0.120 17 45727828 intron variant T/C;G snv 0.60
CUI: C0393571
Disease: Multiple System Atrophy
Multiple System Atrophy 		0.700 1.000 1 2016 2016