rs1448674651
|
0.667 |
0.560 |
18 |
671384 |
missense variant |
G/A;C
|
snv
|
4.0E-06
|
|
Coronary Artery Disease
|
Cardiovascular Diseases
|
0.020 |
1.000 |
2 |
2013 |
2015 |
rs34743033
|
0.776 |
0.200 |
18 |
657657 |
5 prime UTR variant |
GGCCTGCCTCCGTCCCGCCGCGCCACTTGGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCCC/CGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCG;CGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCG;CGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCG
|
delins
|
|
|
Stomatitis
|
Stomatognathic Diseases
|
0.020 |
0.500 |
2 |
2013 |
2018 |
rs1448674651
|
0.667 |
0.560 |
18 |
671384 |
missense variant |
G/A;C
|
snv
|
4.0E-06
|
|
Coronary heart disease
|
Cardiovascular Diseases
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs2853533
|
1.000 |
0.080 |
18 |
658064 |
non coding transcript exon variant |
G/C
|
snv
|
0.22
|
0.22
|
Colorectal Carcinoma
|
Digestive System Diseases; Neoplasms
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs34743033
|
0.776 |
0.200 |
18 |
657657 |
5 prime UTR variant |
GGCCTGCCTCCGTCCCGCCGCGCCACTTGGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCCC/CGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCG;CGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCG;CGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCG
|
delins
|
|
|
Colorectal Carcinoma
|
Digestive System Diseases; Neoplasms
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs1448674651
|
0.667 |
0.560 |
18 |
671384 |
missense variant |
G/A;C
|
snv
|
4.0E-06
|
|
Lupus Erythematosus, Systemic
|
Skin and Connective Tissue Diseases; Immune System Diseases
|
0.020 |
1.000 |
2 |
2014 |
2015 |
rs1448674651
|
0.667 |
0.560 |
18 |
671384 |
missense variant |
G/A;C
|
snv
|
4.0E-06
|
|
Neuroblastoma
|
Neoplasms
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs1448674651
|
0.667 |
0.560 |
18 |
671384 |
missense variant |
G/A;C
|
snv
|
4.0E-06
|
|
Central neuroblastoma
|
Neoplasms; Nervous System Diseases
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs1448674651
|
0.667 |
0.560 |
18 |
671384 |
missense variant |
G/A;C
|
snv
|
4.0E-06
|
|
Childhood Neuroblastoma
|
Neoplasms
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs1059394
|
0.925 |
0.080 |
18 |
672792 |
3 prime UTR variant |
C/T
|
snv
|
|
0.40
|
Sporadic Breast Carcinoma
|
Neoplasms; Skin and Connective Tissue Diseases
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs1448674651
|
0.667 |
0.560 |
18 |
671384 |
missense variant |
G/A;C
|
snv
|
4.0E-06
|
|
Parkinson Disease
|
Nervous System Diseases
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs1448674651
|
0.667 |
0.560 |
18 |
671384 |
missense variant |
G/A;C
|
snv
|
4.0E-06
|
|
Turner Syndrome
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases; Cardiovascular Diseases
|
0.010 |
< 0.001 |
1 |
2015 |
2015 |
rs2790
|
0.925 |
0.160 |
18 |
673086 |
3 prime UTR variant |
A/G;T
|
snv
|
|
0.22
|
Sporadic Breast Carcinoma
|
Neoplasms; Skin and Connective Tissue Diseases
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs2847153
|
0.925 |
0.080 |
18 |
661647 |
intron variant |
G/A
|
snv
|
|
0.22
|
Non-Small Cell Lung Carcinoma
|
Neoplasms; Respiratory Tract Diseases
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs34743033
|
0.776 |
0.200 |
18 |
657657 |
5 prime UTR variant |
GGCCTGCCTCCGTCCCGCCGCGCCACTTGGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCCC/CGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCG;CGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCG;CGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCG
|
delins
|
|
|
Neutropenia
|
Hemic and Lymphatic Diseases
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs34743033
|
0.776 |
0.200 |
18 |
657657 |
5 prime UTR variant |
GGCCTGCCTCCGTCCCGCCGCGCCACTTGGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCCC/CGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCG;CGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCG;CGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCG
|
delins
|
|
|
Leukopenia
|
Hemic and Lymphatic Diseases
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs34743033
|
0.776 |
0.200 |
18 |
657657 |
5 prime UTR variant |
GGCCTGCCTCCGTCCCGCCGCGCCACTTGGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCCC/CGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCG;CGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCG;CGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCG
|
delins
|
|
|
Retinoblastoma
|
Neoplasms; Eye Diseases
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs66567989
|
|
|
18 |
660442 |
intron variant |
A/-
|
del
|
|
0.11
|
Mean Corpuscular Volume (result)
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs66567989
|
|
|
18 |
660442 |
intron variant |
A/-
|
del
|
|
0.11
|
Finding of Mean Corpuscular Hemoglobin
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs34743033
|
0.776 |
0.200 |
18 |
657657 |
5 prime UTR variant |
GGCCTGCCTCCGTCCCGCCGCGCCACTTGGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCCC/CGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCG;CGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCG;CGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCG
|
delins
|
|
|
Stomach Carcinoma
|
Digestive System Diseases; Neoplasms
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs34743033
|
0.776 |
0.200 |
18 |
657657 |
5 prime UTR variant |
GGCCTGCCTCCGTCCCGCCGCGCCACTTGGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCCC/CGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCG;CGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCG;CGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCGCCGCGCCACTTCGCCTGCCTCCGTCCCG
|
delins
|
|
|
Malignant neoplasm of stomach
|
Digestive System Diseases; Neoplasms
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs9967368
|
1.000 |
0.080 |
18 |
656020 |
intron variant |
C/G;T
|
snv
|
|
|
Liver carcinoma
|
Digestive System Diseases; Neoplasms
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs1001761
|
1.000 |
0.080 |
18 |
662103 |
intron variant |
G/A
|
snv
|
0.50
|
0.55
|
Skin lesion
|
Skin and Connective Tissue Diseases
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs151264360
|
0.925 |
0.040 |
18 |
673444 |
3 prime UTR variant |
AAGTTA/-;AAGTTAAAGTTA
|
delins
|
|
|
Oral Mucositis
|
Stomatognathic Diseases
|
0.010 |
< 0.001 |
1 |
2018 |
2018 |
rs151264360
|
0.925 |
0.040 |
18 |
673444 |
3 prime UTR variant |
AAGTTA/-;AAGTTAAAGTTA
|
delins
|
|
|
Hyponatremia
|
Nutritional and Metabolic Diseases
|
0.010 |
1.000 |
1 |
2018 |
2018 |