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: rs6738825
rs6738825
PLCL1
0.851 0.200 2 198032171 intron variant A/G snv 0.49
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 2 2010 2017
dbSNP: rs1016883
rs1016883
PLCL1
1.000 0.040 2 198016944 intron variant G/A snv 0.20
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.800 1.000 1 2012 2012
dbSNP: rs10497813
rs10497813
PLCL1
2 198049348 intron variant G/T snv 0.43
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.800 1.000 1 2013 2013
dbSNP: rs1064213
rs1064213
PLCL1
2 198085516 missense variant G/A snv 0.44 0.41
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.800 1.000 1 2013 2017
dbSNP: rs7421388
rs7421388
PLCL1
0.925 0.080 2 198223806 intron variant A/C;G snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.710 1.000 1 2016 2016
dbSNP: rs1837495
rs1837495
PLCL1
1.000 0.040 2 198056477 intron variant G/A snv 0.61
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 2 2015 2019
dbSNP: rs1025549
rs1025549
PLCL1
1.000 0.040 2 198016459 intron variant G/A;T snv
CUI: C0013595
Disease: Eczema
Eczema 		0.700 1.000 1 2019 2019
dbSNP: rs1036336
rs1036336
PLCL1
2 198099396 intron variant T/C snv 0.45
CUI: C0337443
Disease: Sodium measurement
Sodium measurement 		0.700 1.000 1 2019 2019
dbSNP: rs1064213
rs1064213
PLCL1
2 198085516 missense variant G/A snv 0.44 0.41
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs1147169
rs1147169
PLCL1
2 198036671 intron variant T/C snv 0.67
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2016 2016
dbSNP: rs11684176
rs11684176
PLCL1
2 198090050 intron variant C/T snv 0.38
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms 		0.700 1.000 1 2016 2016
dbSNP: rs11684176
rs11684176
PLCL1
2 198090050 intron variant C/T snv 0.38
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs11896635
rs11896635
PLCL1 ; LOC105373831
0.925 0.040 2 198514620 intron variant T/C snv 0.11
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs11896635
rs11896635
PLCL1 ; LOC105373831
0.925 0.040 2 198514620 intron variant T/C snv 0.11
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs1440088
rs1440088
PLCL1
1.000 0.040 2 198006693 intron variant T/G snv 0.21
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2015 2015
dbSNP: rs1531180
rs1531180
PLCL1
2 198232430 intron variant G/A snv 0.57
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs1595824
rs1595824
PLCL1
2 198009282 intron variant C/A;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs1595824
rs1595824
PLCL1
2 198009282 intron variant C/A;T snv
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms 		0.700 1.000 1 2016 2016
dbSNP: rs1595825
rs1595825
PLCL1
1.000 0.040 2 198010740 intron variant G/A snv 0.23
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2015 2015
dbSNP: rs2164068
rs2164068
PLCL1
1.000 0.120 2 198079128 intron variant T/A snv 0.52
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs2164068
rs2164068
PLCL1
1.000 0.120 2 198079128 intron variant T/A snv 0.52
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2016 2016
dbSNP: rs2164068
rs2164068
PLCL1
1.000 0.120 2 198079128 intron variant T/A snv 0.52
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		0.700 1.000 1 2018 2018
dbSNP: rs2196171
rs2196171
PLCL1
1.000 0.080 2 198025083 intron variant T/A;G snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2017 2017
dbSNP: rs4502401
rs4502401
PLCL1
2 198458802 intron variant T/C snv 0.33
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs4850817
rs4850817
PLCL1
2 197930480 intron variant A/G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018