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: rs35441874
rs35441874
CLEC16A
0.882 0.120 16 11119164 intron variant T/A snv 0.19
CUI: C0741260
Disease: Adult onset asthma
Adult onset asthma 		0.700 1.000 1 2019 2019
dbSNP: rs35441874
rs35441874
CLEC16A
0.882 0.120 16 11119164 intron variant T/A snv 0.19
CUI: C0013595
Disease: Eczema
Eczema 		0.700 1.000 1 2019 2019
dbSNP: rs36045143
rs36045143
CLEC16A ; LOC105371081
1.000 0.080 16 11131109 intron variant A/G snv 0.18
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs36045143
rs36045143
CLEC16A ; LOC105371081
1.000 0.080 16 11131109 intron variant A/G snv 0.18
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2018 2018
dbSNP: rs36045143
rs36045143
CLEC16A ; LOC105371081
1.000 0.080 16 11131109 intron variant A/G snv 0.18
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2018 2018
dbSNP: rs3862469
rs3862469
CLEC16A
1.000 0.040 16 11100223 intron variant C/T snv 0.35
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata 		0.700 1.000 1 2015 2015
dbSNP: rs62026377
rs62026377
CLEC16A ; LOC105371081
16 11135271 intron variant G/T snv 0.23
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs6498142
rs6498142
CLEC16A
16 10987392 intron variant C/G snv 0.77
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2010 2010
dbSNP: rs6498160
rs6498160
CLEC16A
1.000 0.080 16 11105590 intron variant T/C snv 0.51
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2017 2017
dbSNP: rs6498168
rs6498168
CLEC16A
1.000 0.080 16 11141273 intron variant T/G snv 0.71
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2016 2016
dbSNP: rs7200786
rs7200786
CLEC16A
0.882 0.200 16 11083944 intron variant A/G snv 0.59
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2015 2015
dbSNP: rs725613
rs725613
CLEC16A
0.851 0.240 16 11075826 intron variant T/G snv 0.42
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2017 2017
dbSNP: rs8054198
rs8054198
CLEC16A
1.000 0.080 16 10944503 upstream gene variant C/T snv 6.7E-02
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2017 2017
dbSNP: rs8061043
rs8061043
CLEC16A
16 11067072 intron variant G/T snv 0.19
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs8061882
rs8061882
CLEC16A
0.827 0.120 16 11067551 intron variant G/C snv 0.11
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs8061882
rs8061882
CLEC16A
0.827 0.120 16 11067551 intron variant G/C snv 0.11
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs8061882
rs8061882
CLEC16A
0.827 0.120 16 11067551 intron variant G/C snv 0.11
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016
dbSNP: rs8061882
rs8061882
CLEC16A
0.827 0.120 16 11067551 intron variant G/C snv 0.11
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs8061882
rs8061882
CLEC16A
0.827 0.120 16 11067551 intron variant G/C snv 0.11
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs876476
rs876476
CLEC16A
16 11056391 intron variant G/A snv 0.26
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs887864
rs887864
CLEC16A
0.925 0.120 16 11065028 intron variant G/A;C;T snv
CUI: C0018621
Disease: Hay fever
Hay fever 		0.700 1.000 1 2011 2011
dbSNP: rs9923856
rs9923856
CLEC16A
1.000 0.080 16 11116558 intron variant T/C snv 0.41
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2017 2017
dbSNP: rs62026376
rs62026376
CLEC16A ; LOC105371081
0.925 0.120 16 11134855 intron variant C/T snv 0.18
CUI: C0004096
Disease: Asthma
Asthma 		0.710 1.000 1 2014 2014
dbSNP: rs62026376
rs62026376
CLEC16A ; LOC105371081
0.925 0.120 16 11134855 intron variant C/T snv 0.18
CUI: C0018621
Disease: Hay fever
Hay fever 		0.710 1.000 1 2014 2014
dbSNP: rs12708716
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.800 1.000 5 2007 2011