rs113488022, BRAF

N. diseases: 490
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.
ASTROCYTOMA, LOW-GRADE, SOMATIC
CUI: C2674727
Disease: ASTROCYTOMA, LOW-GRADE, SOMATIC
1 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.700 0
Nongerminomatous Germ Cell Tumor
CUI: C1266158
Disease: Nongerminomatous Germ Cell Tumor
1 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.700 0
Adult Fibrosarcoma
CUI: C0278595
Disease: Adult Fibrosarcoma
9 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2003 2003
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2003 2003
Fibrosarcoma
CUI: C0016057
Disease: Fibrosarcoma
9 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2003 2003
Hereditary Melanoma
CUI: C1512419
Disease: Hereditary Melanoma
67 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1 2003 2003
Nodular Goiter
CUI: C0018023
Disease: Nodular Goiter
12 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2003 2003
Precancerous Conditions
CUI: C0032927
Disease: Precancerous Conditions
18 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2003 2003
Carcinoid tumor, malignant
CUI: C0391970
Disease: Carcinoid tumor, malignant
2 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2004 2004
endocrine carcinoma
CUI: C0848860
Disease: endocrine carcinoma
2 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2004 2004
Familial Nonmedullary Thyroid Cancer
2 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2005 2005
Hereditary nonpolyposis colorectal carcinoma
5 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2005 2005
Nevi and Melanomas
CUI: C0206769
Disease: Nevi and Melanomas
3 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2005 2005
Human immunodeficiency virus (HIV) II infection category B1
56 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2006 2006
Malignant melanoma of choroid
CUI: C0346388
Disease: Malignant melanoma of choroid
5 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2006 2006
Merkel cell carcinoma
CUI: C0007129
Disease: Merkel cell carcinoma
10 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1 2006 2006
premalignant lesion
CUI: C0850639
Disease: premalignant lesion
5 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2006 2006
Adenomatous Polyposis Coli
CUI: C0032580
Disease: Adenomatous Polyposis Coli
237 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1 2007 2007
Keratosis
CUI: C0022593
Disease: Keratosis
10 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2007 2007
Malignant melanoma of iris
CUI: C0346373
Disease: Malignant melanoma of iris
1 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2007 2007
Multiple Chronic Conditions
CUI: C3266262
Disease: Multiple Chronic Conditions
42 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2007 2007
Ovarian Carcinoma
CUI: C0029925
Disease: Ovarian Carcinoma
19 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2007 2007
Papillary serous cystadenocarcinoma
CUI: C0334359
Disease: Papillary serous cystadenocarcinoma
2 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2007 2007
Thyroid Diseases
CUI: C0040128
Disease: Thyroid Diseases
26 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.010 1.000 1 2007 2007
Anthrax disease
CUI: C0003175
Disease: Anthrax disease
3 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.030 1.000 3 2005 2008