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: rs116855232
rs116855232
0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02
CUI: C0023530
Disease: Leukopenia
Leukopenia
0.800 1.000 3 2014 2020
dbSNP: rs116855232
rs116855232
0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.750 1.000 2 2016 2019
dbSNP: rs116855232
rs116855232
0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02
CUI: C0002170
Disease: Alopecia
Alopecia
0.750 1.000 1 2016 2018
dbSNP: rs116855232
rs116855232
0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.730 1.000 1 2014 2018