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: rs1372072
rs1372072
PLCL2
0.851 0.200 3 16913767 intron variant G/A snv 0.35
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.800 1.000 2 2011 2015
dbSNP: rs4452313
rs4452313
PLCL2
1.000 0.120 3 17005540 intron variant A/T snv 0.40
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.800 1.000 2 2014 2019
dbSNP: rs4618210
rs4618210
PLCL2
1.000 0.080 3 17082892 intron variant A/G snv 0.56
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.800 1.000 1 2015 2015
dbSNP: rs73139272
rs73139272
PLCL2
3 16816965 intron variant G/A;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 2 2018 2018
dbSNP: rs748832
rs748832
PLCL2
3 16809700 intron variant G/A snv 0.59
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 2 2017 2019
dbSNP: rs9821630
rs9821630
PLCL2
3 16929446 intron variant A/G snv 0.24
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 2 2016 2017
dbSNP: rs114893614
rs114893614
PLCL2
3 16891211 intron variant C/T snv 4.1E-02
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs114893614
rs114893614
PLCL2
3 16891211 intron variant C/T snv 4.1E-02
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs115792481
rs115792481
PLCL2
3 16898659 intron variant G/T snv 4.6E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2018 2018
dbSNP: rs116577908
rs116577908
PLCL2
3 17056907 intron variant A/G snv 7.1E-03
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs116577908
rs116577908
PLCL2
3 17056907 intron variant A/G snv 7.1E-03
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs116577908
rs116577908
PLCL2
3 17056907 intron variant A/G snv 7.1E-03
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs116577908
rs116577908
PLCL2
3 17056907 intron variant A/G snv 7.1E-03
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs1372072
rs1372072
PLCL2
0.851 0.200 3 16913767 intron variant G/A snv 0.35
CUI: C0023892
Disease: Biliary cirrhosis
Biliary cirrhosis 		0.700 1.000 1 2011 2011
dbSNP: rs143759545
rs143759545
PLCL2 ; LOC105376972
3 16884567 intron variant C/G;T snv
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs144614991
rs144614991
PLCL2
3 16925189 intron variant C/T snv 3.9E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1992381
rs1992381
PLCL2 ; LOC105376972
3 16886567 intron variant T/A;C snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs200726463
rs200726463
PLCL2
3 16992491 intron variant -/AG delins 7.1E-03
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs2060597
rs2060597
PLCL2
3 16847490 intron variant T/C snv 3.5E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2017 2017
dbSNP: rs2278609
rs2278609
PLCL2 ; LOC105376972
1.000 0.040 3 16882947 intron variant C/A;G;T snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs2278609
rs2278609
PLCL2 ; LOC105376972
1.000 0.040 3 16882947 intron variant C/A;G;T snv
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs4685408
rs4685408
PLCL2
0.925 0.040 3 16954543 intron variant G/A snv 0.56
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2015 2015
dbSNP: rs4685408
rs4685408
PLCL2
0.925 0.040 3 16954543 intron variant G/A snv 0.56
CUI: C0263361
Disease: Psoriasis vulgaris
Psoriasis vulgaris 		0.700 1.000 1 2015 2015
dbSNP: rs6779302
rs6779302
PLCL2
3 16818207 intron variant T/A;G snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2017 2017
dbSNP: rs6804663
rs6804663
PLCL2
1.000 0.040 3 16833950 intron variant G/A snv 0.58
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018