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: 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: 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: 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: 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: 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: rs9652601
rs9652601
CLEC16A
1.000 0.080 16 11080508 intron variant G/A snv 0.34
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 3 2015 2017
dbSNP: rs7203459
rs7203459
CLEC16A ; LOC105371081
1.000 0.080 16 11136846 intron variant T/C snv 0.23
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 2 2016 2019
dbSNP: rs11645657
rs11645657
CLEC16A ; LOC105371081
1.000 0.080 16 11129597 intron variant C/A;G snv 0.48
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2018 2018
dbSNP: rs11645657
rs11645657
CLEC16A ; LOC105371081
1.000 0.080 16 11129597 intron variant C/A;G snv 0.48
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2018 2018
dbSNP: rs11865121
rs11865121
CLEC16A
1.000 0.080 16 11072831 intron variant C/A snv 0.40
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.800 1.000 1 2009 2009
dbSNP: rs12708715
rs12708715
CLEC16A
1.000 0.080 16 11083967 intron variant C/T snv 0.39
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.800 1.000 1 2012 2012
dbSNP: rs12935413
rs12935413
CLEC16A
1.000 0.080 16 11116590 intron variant G/A snv 0.34
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs12935413
rs12935413
CLEC16A
1.000 0.080 16 11116590 intron variant G/A snv 0.34
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs12935657
rs12935657
CLEC16A
0.925 0.080 16 11125184 intron variant G/A snv 0.18
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		0.700 1.000 1 2019 2019
dbSNP: rs12935657
rs12935657
CLEC16A
0.925 0.080 16 11125184 intron variant G/A snv 0.18
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
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: 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: 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: 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: 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