rs1057910, CYP2C9

N. diseases: 12
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 0.030 1.000 3 2007 2014
Leukopenia
CUI: C0023530
Disease: Leukopenia
153 0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 0.020 1.000 2 2014 2017
Absence of sensation
CUI: C0278134
Disease: Absence of sensation
5 0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 0.010 1.000 1 2017 2017
Acute gastrointestinal hemorrhage
CUI: C0266807
Disease: Acute gastrointestinal hemorrhage
4 0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 0.010 1.000 1 2009 2009
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 0.010 1.000 1 2006 2006
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 0.010 1.000 1 2014 2014
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 0.010 1.000 1 2016 2016
Diarrhea
CUI: C0011991
Disease: Diarrhea
63 0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 0.010 1.000 1 2017 2017
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 0.010 1.000 1 1998 1998
Neutropenia
CUI: C0027947
Disease: Neutropenia
97 0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 0.010 1.000 1 2017 2017
Thrombophilia
CUI: C0398623
Disease: Thrombophilia
43 0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 0.010 1.000 1 2019 2019
WARFARIN SENSITIVITY (disorder)
CUI: C2608079
Disease: WARFARIN SENSITIVITY (disorder)
8 0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 0.010 1.000 1 2019 2019