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: rs6804663
rs6804663
PLCL2
1.000 0.040 3 16833950 intron variant G/A snv 0.58
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs73139274
rs73139274
PLCL2
3 16817019 intron variant C/G snv 0.16
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs73146904
rs73146904
PLCL2
3 16891490 intron variant G/A snv 9.4E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs73146904
rs73146904
PLCL2
3 16891490 intron variant G/A snv 9.4E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs73146904
rs73146904
PLCL2
3 16891490 intron variant G/A snv 9.4E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs75885714
rs75885714
PLCL2
3 16901018 intron variant A/C snv 4.6E-02
CUI: C2697758
Disease: Interleukin 10 Measurement
Interleukin 10 Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs75885714
rs75885714
PLCL2
3 16901018 intron variant A/C snv 4.6E-02
CUI: C3897558
Disease: Soluble Interleukin 6 Receptor Measurement
Soluble Interleukin 6 Receptor Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs75885714
rs75885714
PLCL2
3 16901018 intron variant A/C snv 4.6E-02
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs75885714
rs75885714
PLCL2
3 16901018 intron variant A/C snv 4.6E-02
CUI: C3815172
Disease: Interleukin 1 Beta Measurement
Interleukin 1 Beta Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs75885714
rs75885714
PLCL2
3 16901018 intron variant A/C snv 4.6E-02
CUI: C2825877
Disease: Interferon Gamma Measurement
Interferon Gamma Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs75885714
rs75885714
PLCL2
3 16901018 intron variant A/C snv 4.6E-02
CUI: C2697779
Disease: Interleukin 2 Measurement
Interleukin 2 Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs75885714
rs75885714
PLCL2
3 16901018 intron variant A/C snv 4.6E-02
CUI: C4318750
Disease: Chemokine (C-C Motif) Ligand 19 Measurement
Chemokine (C-C Motif) Ligand 19 Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7613595
rs7613595
PLCL2
3 16867007 intron variant C/A snv 0.79
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs7613595
rs7613595
PLCL2
3 16867007 intron variant C/A snv 0.79
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs7653834
rs7653834
PLCL2
0.925 0.040 3 17009836 synonymous variant T/C snv 0.37 0.38
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs7653834
rs7653834
PLCL2
0.925 0.040 3 17009836 synonymous variant T/C snv 0.37 0.38
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs79638618
rs79638618
PLCL2
3 16890061 intron variant C/T snv 3.7E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2018 2018
dbSNP: rs9813513
rs9813513
PLCL2
3 16815180 intron variant C/T snv 0.58
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs9821630
rs9821630
PLCL2
3 16929446 intron variant A/G snv 0.24
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs9846711
rs9846711
PLCL2
1.000 0.040 3 16821370 intron variant T/C snv 0.58
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2019 2019
dbSNP: rs9846711
rs9846711
PLCL2
1.000 0.040 3 16821370 intron variant T/C snv 0.58
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs9852648
rs9852648
PLCL2
3 16869827 intron variant G/A snv 0.76
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs9858071
rs9858071
PLCL2
1.000 0.040 3 16803898 intron variant T/C snv 0.37
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs9858071
rs9858071
PLCL2
1.000 0.040 3 16803898 intron variant T/C snv 0.37
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018