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: 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: 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: rs11644510
rs11644510
CLEC16A
1.000 0.120 16 11183501 downstream gene variant C/T snv 0.39
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 2 2016 2017
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: 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: 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: 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: 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: rs11644510
rs11644510
CLEC16A
1.000 0.120 16 11183501 downstream gene variant C/T snv 0.39
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		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: 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: 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: 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: 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: 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: rs12924112
rs12924112
CLEC16A
1.000 0.120 16 11125863 intron variant T/A;G snv
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis 		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: 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: 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