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
|
|
|
Oral Mucositis
|
Stomatognathic Diseases
|
0.010 |
< 0.001 |
1 |
2018 |
2018 |
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 |
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
|
|
|
Malignant neoplasm of stomach
|
Digestive System Diseases; Neoplasms
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs502396
|
1.000 |
0.080 |
18 |
659236 |
intron variant |
C/T
|
snv
|
|
0.46
|
Spina Bifida
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs502396
|
1.000 |
0.080 |
18 |
659236 |
intron variant |
C/T
|
snv
|
|
0.46
|
Neural Tube Defects
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs699517
|
|
|
18 |
673016 |
3 prime UTR variant |
C/T
|
snv
|
0.38
|
0.40
|
Neural Tube Defects
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs750248338
|
0.925 |
0.080 |
18 |
670857 |
missense variant |
C/T
|
snv
|
4.0E-06
|
|
Colorectal Carcinoma
|
Digestive System Diseases; Neoplasms
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs750248338
|
0.925 |
0.080 |
18 |
670857 |
missense variant |
C/T
|
snv
|
4.0E-06
|
|
Malignant neoplasm of colon and/or rectum
|
|
0.010 |
1.000 |
1 |
2018 |
2018 |
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 |