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: 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
dbSNP: rs2903692
rs2903692
CLEC16A
0.807 0.360 16 11144926 intron variant G/A snv 0.33
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.840 1.000 1 2007 2010
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: 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: 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: rs12924729
rs12924729
CLEC16A
0.882 0.200 16 11093926 intron variant G/A snv 0.34
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.800 1.000 2 2011 2015
dbSNP: rs35441874
rs35441874
CLEC16A
0.882 0.120 16 11119164 intron variant T/A snv 0.19
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 2 2019 2019
dbSNP: rs12924729
rs12924729
CLEC16A
0.882 0.200 16 11093926 intron variant G/A snv 0.34
CUI: C0023892
Disease: Biliary cirrhosis
Biliary cirrhosis 		0.700 1.000 1 2011 2011
dbSNP: rs12927355
rs12927355
CLEC16A
0.882 0.240 16 11100914 intron variant C/A;T snv 0.29
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.800 1.000 1 2011 2015
dbSNP: rs12927355
rs12927355
CLEC16A
0.882 0.240 16 11100914 intron variant C/A;T snv 0.29
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2013 2013
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: 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: rs7200786
rs7200786
CLEC16A
0.882 0.200 16 11083944 intron variant A/G snv 0.59
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.800 1.000 1 2011 2011
dbSNP: rs12599402
rs12599402
CLEC16A
0.925 0.160 16 11096031 intron variant T/C snv 0.51
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.810 1.000 1 2011 2013
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