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 |
rs2853741
|
1.000 |
0.080 |
18 |
657352 |
intron variant |
T/C;G
|
snv
|
|
|
Hyalinosis, Systemic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs2606241
|
1.000 |
0.080 |
18 |
657443 |
intron variant |
A/C
|
snv
|
|
0.66
|
Hyalinosis, Systemic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
|
0.010 |
1.000 |
1 |
2019 |
2019 |
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 |
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
|
|
|
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
|
|
|
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 |
rs2853542
|
1.000 |
0.120 |
18 |
657685 |
5 prime UTR variant |
G/C;T
|
snv
|
|
|
Childhood Acute Lymphoblastic Leukemia
|
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
|
0.010 |
1.000 |
1 |
2018 |
2018 |
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 |
rs3891167
|
|
|
18 |
658423 |
non coding transcript exon variant |
A/G
|
snv
|
|
0.26
|
Finding of Mean Corpuscular Hemoglobin
|
|
0.700 |
1.000 |
1 |
2019 |
2019 |
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 |
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 |
rs2847153
|
0.925 |
0.080 |
18 |
661647 |
intron variant |
G/A
|
snv
|
|
0.22
|
Glioma
|
Neoplasms
|
0.020 |
1.000 |
2 |
2019 |
2019 |
rs2847153
|
0.925 |
0.080 |
18 |
661647 |
intron variant |
G/A
|
snv
|
|
0.22
|
Lymphocyte Count measurement
|
|
0.700 |
1.000 |
1 |
2012 |
2012 |
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 |
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 |
rs1001761
|
1.000 |
0.080 |
18 |
662103 |
intron variant |
G/A
|
snv
|
0.50
|
0.55
|
Spina Bifida
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs11873890
|
|
|
18 |
662135 |
intron variant |
A/G
|
snv
|
8.2E-03
|
3.2E-02
|
High density lipoprotein measurement
|
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs11873890
|
|
|
18 |
662135 |
intron variant |
A/G
|
snv
|
8.2E-03
|
3.2E-02
|
Triglycerides measurement
|
|
0.700 |
1.000 |
1 |
2012 |
2012 |