Source: BEFREE

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: rs4444903
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51
CUI: C0239946
Disease: Fibrosis, Liver
Fibrosis, Liver
0.010 1.000 1 2012 2012
dbSNP: rs4444903
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51
CUI: C0235782
Disease: Gallbladder Carcinoma
Gallbladder Carcinoma
0.010 1.000 1 2008 2008
dbSNP: rs4444903
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51
Stage IIA Gallbladder Cancer AJCC v8
0.010 1.000 1 2008 2008
dbSNP: rs4444903
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51
CUI: C3665419
Disease: intracranial glioma
intracranial glioma
0.010 1.000 1 2010 2010
dbSNP: rs4444903
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.010 1.000 1 2018 2018
dbSNP: rs4444903
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 1.000 1 2014 2014
dbSNP: rs4444903
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51
Malignant neoplasm of gastrointestinal tract
0.010 1.000 1 2013 2013
dbSNP: rs4444903
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.010 1.000 1 2012 2012
dbSNP: rs4444903
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51
CUI: C4525305
Disease: Stage IV Gallbladder Cancer AJCC v8
Stage IV Gallbladder Cancer AJCC v8
0.010 1.000 1 2008 2008
dbSNP: rs4444903
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51
Stage IIB Gallbladder Cancer AJCC v8
0.010 1.000 1 2008 2008
dbSNP: rs4444903
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.010 1.000 1 2005 2005
dbSNP: rs4444903
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51
Conventional (Clear Cell) Renal Cell Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs4444903
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs4444903
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.010 1.000 1 2012 2012
dbSNP: rs4444903
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2013 2013
dbSNP: rs4444903
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51
CUI: C0276623
Disease: Chronic viral hepatitis
Chronic viral hepatitis
0.010 1.000 1 2012 2012
dbSNP: rs4444903
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51
CUI: C4525297
Disease: Stage 0 Gallbladder Cancer AJCC v8
Stage 0 Gallbladder Cancer AJCC v8
0.010 1.000 1 2008 2008
dbSNP: rs4444903
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51
CUI: C0153452
Disease: Malignant neoplasm of gallbladder
Malignant neoplasm of gallbladder
0.010 1.000 1 2008 2008
dbSNP: rs4444903
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma
0.010 < 0.001 1 2015 2015
dbSNP: rs4444903
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 1.000 1 2005 2005
dbSNP: rs4444903
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51
Stage III Gallbladder Cancer AJCC v8
0.010 1.000 1 2008 2008
dbSNP: rs4698803
rs4698803
EGF
1.000 0.040 4 109993271 missense variant A/G;T snv 0.85
Respiratory Distress Syndrome, Adult
0.010 1.000 1 2009 2009
dbSNP: rs6533485
rs6533485
EGF
1.000 0.040 4 110006407 intron variant G/C snv 0.61
Respiratory Distress Syndrome, Adult
0.010 1.000 1 2009 2009
dbSNP: rs769047429
rs769047429
EGF
1.000 4 109999827 frameshift variant -/G delins 8.0E-06
CUI: C1167791
Disease: Skin toxicity
Skin toxicity
0.010 1.000 1 2010 2010
dbSNP: rs7692976
rs7692976
EGF
1.000 0.040 4 109990411 intron variant A/G;T snv
Respiratory Distress Syndrome, Adult
0.010 1.000 1 2009 2009