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: rs17229044
rs17229044
CLEC16A
1.000 0.120 16 10969079 intron variant C/T snv 0.16
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs17806299
rs17806299
CLEC16A
1.000 0.080 16 11106123 intron variant G/A snv 0.15
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2018 2018
dbSNP: rs2041670
rs2041670
CLEC16A
0.851 0.280 16 11080795 intron variant G/A;C snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2017 2017
dbSNP: rs2041733
rs2041733
CLEC16A ; LOC105371081
1.000 0.120 16 11135732 intron variant T/C;G snv
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		0.700 1.000 1 2015 2015
dbSNP: rs248831
rs248831
CLEC16A
16 11187361 intergenic variant G/A snv 0.31
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs34069391
rs34069391
CLEC16A
0.925 0.080 16 11067358 intron variant T/- delins
CUI: C4049006
Disease: Selective immunoglobulin A deficiency
Selective immunoglobulin A deficiency 		0.700 1.000 1 2016 2016
dbSNP: rs34069391
rs34069391
CLEC16A
0.925 0.080 16 11067358 intron variant T/- delins
CUI: C0162538
Disease: Immunoglobulin A deficiency (disorder)
Immunoglobulin A deficiency (disorder) 		0.700 1.000 1 2016 2016
dbSNP: rs34972832
rs34972832
CLEC16A
0.925 0.120 16 11105081 intron variant G/A;T snv 0.14
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		0.700 1.000 1 2017 2017
dbSNP: rs34972832
rs34972832
CLEC16A
0.925 0.120 16 11105081 intron variant G/A;T snv 0.14
CUI: C0152268
Disease: Nodular Sclerosis Classical Hodgkin Lymphoma
Nodular Sclerosis Classical Hodgkin Lymphoma 		0.700 1.000 1 2017 2017
dbSNP: rs35032408
rs35032408
CLEC16A
0.925 0.080 16 11121567 intron variant T/C;G snv
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		0.700 1.000 1 2019 2019
dbSNP: rs35032408
rs35032408
CLEC16A
0.925 0.080 16 11121567 intron variant T/C;G snv
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: 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