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: rs12712127
rs12712127
2 102110201 intron variant A/G snv 0.62
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.800 1.000 1 2013 2013
dbSNP: rs1558643
rs1558643
2 102115231 intron variant T/C;G snv
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.700 1.000 2 2016 2017
dbSNP: rs13427957
rs13427957
1.000 0.080 2 102072571 intron variant C/T snv 0.46
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
dbSNP: rs150946191
rs150946191
2 102116028 intron variant T/G snv 1.9E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs2228139
rs2228139
2 102165189 missense variant C/A;G snv 5.6E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs3917254
rs3917254
2 102160058 intron variant G/A snv 0.16
Interleukin 1 Receptor-Like 1 Measurement
0.700 1.000 1 2017 2017
dbSNP: rs3917265
rs3917265
1.000 0.120 2 102162001 intron variant T/C snv 0.50
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.700 1.000 1 2015 2015
dbSNP: rs3917265
rs3917265
1.000 0.120 2 102162001 intron variant T/C snv 0.50
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs4141632
rs4141632
2 102140679 intron variant A/G;T snv
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2018 2018
dbSNP: rs4851541
rs4851541
2 102123999 intron variant G/T snv 0.40
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 1 2019 2019
dbSNP: rs7588201
rs7588201
2 102129816 intron variant A/C snv 0.39
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs871656
rs871656
0.827 0.120 2 102154822 intron variant T/A;C snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 1 2016 2016
dbSNP: rs871656
rs871656
0.827 0.120 2 102154822 intron variant T/A;C snv
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2016 2016
dbSNP: rs871656
rs871656
0.827 0.120 2 102154822 intron variant T/A;C snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2016 2016
dbSNP: rs871656
rs871656
0.827 0.120 2 102154822 intron variant T/A;C snv
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
0.700 1.000 1 2016 2016
dbSNP: rs871656
rs871656
0.827 0.120 2 102154822 intron variant T/A;C snv
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 1 2016 2016
dbSNP: rs9284725
rs9284725
2 102128394 intron variant C/A;T snv 0.82
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2018 2018