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: rs2942168
rs2942168
LINC02210 ; LINC02210-CRHR1
0.925 0.120 17 45637484 non coding transcript exon variant G/A;C;T snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.820 1.000 1 2011 2014
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: 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: rs35076622
rs35076622
LINC02210-CRHR1
1.000 0.040 17 45779092 intron variant G/A;C snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 2 2018 2019
dbSNP: rs55657917
rs55657917
LINC02210-CRHR1
17 45767194 intron variant T/G snv 0.14
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 2 2018 2018
dbSNP: rs112550936
rs112550936
LINC02210 ; LINC02210-CRHR1
17 45638789 intron variant A/G snv 0.14
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs12150672
rs12150672
LINC02210-CRHR1
17 45749271 intron variant G/A;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2017 2017
dbSNP: rs12938031
rs12938031
LINC02210-CRHR1
0.851 0.160 17 45777136 intron variant A/G snv 0.26
CUI: C0003467
Disease: Anxiety
Anxiety 		0.700 1.000 1 2018 2018
dbSNP: rs12938031
rs12938031
LINC02210-CRHR1
0.851 0.160 17 45777136 intron variant A/G snv 0.26
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs12938031
rs12938031
LINC02210-CRHR1
0.851 0.160 17 45777136 intron variant A/G snv 0.26
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs12938031
rs12938031
LINC02210-CRHR1
0.851 0.160 17 45777136 intron variant A/G snv 0.26
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs143699161
rs143699161
LINC02210-CRHR1 ; LOC105371802
17 45671346 intron variant A/G snv 0.19
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs143699161
rs143699161
LINC02210-CRHR1 ; LOC105371802
17 45671346 intron variant A/G snv 0.19
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs1526123
rs1526123
LINC02210-CRHR1
1.000 0.040 17 45705974 intron variant T/C snv 0.55
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs1724422
rs1724422
LINC02210-CRHR1
1.000 0.040 17 45699947 intron variant A/G snv 0.47
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs1724422
rs1724422
LINC02210-CRHR1
1.000 0.040 17 45699947 intron variant A/G snv 0.47
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs1724425
rs1724425
LINC02210-CRHR1
17 45704381 intron variant C/T snv 0.40
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs17426174
rs17426174
LINC02210-CRHR1
17 45753572 intron variant G/C snv 0.15
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs17563683
rs17563683
LINC02210-CRHR1 ; LOC107985028
17 45733706 intron variant A/G snv 0.15
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016
dbSNP: rs17563683
rs17563683
LINC02210-CRHR1 ; LOC107985028
17 45733706 intron variant A/G snv 0.15
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs17688916
rs17688916
LINC02210-CRHR1
17 45701314 intron variant T/A snv 0.13
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 1 2019 2019
dbSNP: rs1876829
rs1876829
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
1.000 0.040 17 45834077 intron variant T/C snv 0.15 0.14
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2018 2018
dbSNP: rs241036
rs241036
LINC02210 ; LINC02210-CRHR1
17 45654353 non coding transcript exon variant A/C snv 0.14
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2019 2019
dbSNP: rs34186148
rs34186148
LINC02210-CRHR1
1.000 0.040 17 45777289 intron variant G/A;C snv 0.31
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs34186148
rs34186148
LINC02210-CRHR1
1.000 0.040 17 45777289 intron variant G/A;C snv 0.31
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018