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: rs2038255
rs2038255
14 35089920 intron variant C/T snv 0.19
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs2143950
rs2143950
1.000 0.120 14 35103151 intron variant C/T snv 0.17
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.700 1.000 1 2015 2015
dbSNP: rs4007475
rs4007475
14 35046401 5 prime UTR variant GG/-;G;GGG delins 0.74
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs79403677
rs79403677
0.925 0.040 14 35069925 intron variant T/G snv 0.17
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 1 2018 2018
dbSNP: rs79403677
rs79403677
0.925 0.040 14 35069925 intron variant T/G snv 0.17
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 1.000 1 2018 2018
dbSNP: rs8006884
rs8006884
0.827 0.120 14 35094005 intron variant T/C snv 0.36
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 1 2016 2016
dbSNP: rs8006884
rs8006884
0.827 0.120 14 35094005 intron variant T/C snv 0.36
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
0.700 1.000 1 2016 2016
dbSNP: rs8006884
rs8006884
0.827 0.120 14 35094005 intron variant T/C snv 0.36
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2016 2016
dbSNP: rs8006884
rs8006884
0.827 0.120 14 35094005 intron variant T/C snv 0.36
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2016 2016
dbSNP: rs8006884
rs8006884
0.827 0.120 14 35094005 intron variant T/C snv 0.36
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 1 2016 2016