Source: GWASDB

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: rs6010620
rs6010620
0.701 0.360 20 63678486 intron variant A/C;G snv
CUI: C0017638
Disease: Glioma
Glioma
0.900 0.952 5 2009 2020
dbSNP: rs2297440
rs2297440
0.763 0.080 20 63680946 intron variant T/C snv 0.81
CUI: C0017638
Disease: Glioma
Glioma
0.820 1.000 1 2009 2018
dbSNP: rs6010620
rs6010620
0.701 0.360 20 63678486 intron variant A/C;G snv
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.810 0.667 1 2011 2015
dbSNP: rs6010620
rs6010620
0.701 0.360 20 63678486 intron variant A/C;G snv
CUI: C0085136
Disease: Central Nervous System Neoplasms
Central Nervous System Neoplasms
0.800 1.000 2 2009 2014
dbSNP: rs2297441
rs2297441
0.807 0.160 20 63696229 3 prime UTR variant G/A;C snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.800 1.000 1 2011 2011
dbSNP: rs4809324
rs4809324
0.807 0.200 20 63686867 non coding transcript exon variant T/C snv 8.8E-02
CUI: C0017638
Disease: Glioma
Glioma
0.800 1.000 1 2009 2009
dbSNP: rs4809324
rs4809324
0.807 0.200 20 63686867 non coding transcript exon variant T/C snv 8.8E-02
CUI: C0085136
Disease: Central Nervous System Neoplasms
Central Nervous System Neoplasms
0.800 1.000 1 2009 2009
dbSNP: rs2297441
rs2297441
0.807 0.160 20 63696229 3 prime UTR variant G/A;C snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.710 1.000 1 2008 2009
dbSNP: rs4809324
rs4809324
0.807 0.200 20 63686867 non coding transcript exon variant T/C snv 8.8E-02
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.700 1.000 1 2010 2010
dbSNP: rs6010620
rs6010620
0.701 0.360 20 63678486 intron variant A/C;G snv
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.700 1.000 1 2010 2010