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: 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: 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: 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: 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: rs7203459
rs7203459
CLEC16A ; LOC105371081
1.000 0.080 16 11136846 intron variant T/C snv 0.23
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.800 1.000 1 2013 2013
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: 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: 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: 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: 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: 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: 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: 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: 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: 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: 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: 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: 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: 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: 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: 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: 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