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: rs763361
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.900 0.917 2 2007 2015
dbSNP: rs12969657
rs12969657
CD226
18 69869260 intron variant C/T snv 0.41
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2011 2011
dbSNP: rs2469434
rs2469434
CD226
1.000 0.120 18 69876810 intron variant T/C snv 0.44
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.800 1.000 1 2014 2014
dbSNP: rs727088
rs727088
CD226
0.790 0.400 18 69863203 3 prime UTR variant G/A snv 0.47
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.800 1.000 1 2012 2012
dbSNP: rs893001
rs893001
CD226
18 69849610 intron variant A/C snv 0.18
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2009 2012
dbSNP: rs1788097
rs1788097
CD226
0.925 0.040 18 69876452 intron variant C/T snv 0.56
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 2 2013 2017
dbSNP: rs1615504
rs1615504
CD226
1.000 0.120 18 69859408 3 prime UTR variant T/C snv 0.46
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 1.000 1 2015 2015
dbSNP: rs17207042
rs17207042
CD226
18 69870115 intron variant T/C snv 0.40
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 1 2015 2015
dbSNP: rs1788103
rs1788103
CD226
18 69871588 intron variant A/G snv 0.56
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs1788105
rs1788105
CD226
18 69865056 intron variant A/C;G;T snv
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs1790588
rs1790588
CD226
0.882 18 69867948 intron variant T/C snv 0.55
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs1790588
rs1790588
CD226
0.882 18 69867948 intron variant T/C snv 0.55
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2019 2019
dbSNP: rs1790588
rs1790588
CD226
0.882 18 69867948 intron variant T/C snv 0.55
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2019 2019
dbSNP: rs1790588
rs1790588
CD226
0.882 18 69867948 intron variant T/C snv 0.55
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2019 2019
dbSNP: rs1790963
rs1790963
CD226
18 69851968 intron variant C/A snv 0.47
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs1823778
rs1823778
CD226
18 69934400 intron variant G/C snv 0.67
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs1865761
rs1865761
CD226
18 69872156 intron variant T/C snv 0.41
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs35977166
rs35977166
CD226
18 69862729 3 prime UTR variant CACT/-;CACTCACT delins
CUI: C3828530
Disease: Platelet Component Distribution Width Measurement
Platelet Component Distribution Width Measurement 		0.700 1.000 1 2016 2016
dbSNP: rs4891786
rs4891786
CD226
0.925 0.040 18 69904374 intron variant C/G;T snv
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs4891786
rs4891786
CD226
0.925 0.040 18 69904374 intron variant C/G;T snv
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs66504140
rs66504140
CD226
0.827 0.120 18 69894282 intron variant G/A snv 0.47
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016
dbSNP: rs66504140
rs66504140
CD226
0.827 0.120 18 69894282 intron variant G/A snv 0.47
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs66504140
rs66504140
CD226
0.827 0.120 18 69894282 intron variant G/A snv 0.47
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs66504140
rs66504140
CD226
0.827 0.120 18 69894282 intron variant G/A snv 0.47
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs66504140
rs66504140
CD226
0.827 0.120 18 69894282 intron variant G/A snv 0.47
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016