rs9841504
|
0.827 |
0.120 |
3 |
114643917 |
intron variant |
C/G;T
|
snv
|
|
|
Intestinal metaplasia
|
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs149509568
|
1.000 |
0.040 |
3 |
114316541 |
mature miRNA variant |
A/G
|
snv
|
4.0E-06
|
4.9E-05
|
Keratoconus
|
Eye Diseases
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs139459337
|
0.882 |
0.040 |
3 |
114997018 |
intron variant |
C/T
|
snv
|
|
4.7E-02
|
Major Depressive Disorder
|
Mental Disorders
|
0.700 |
1.000 |
1 |
2018 |
2018 |
rs9841504
|
0.827 |
0.120 |
3 |
114643917 |
intron variant |
C/G;T
|
snv
|
|
|
Malignant neoplasm of esophagus
|
Digestive System Diseases; Neoplasms
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs10511330
|
0.776 |
0.080 |
3 |
114402172 |
intron variant |
T/C
|
snv
|
|
0.22
|
Malignant neoplasm of large intestine
|
Digestive System Diseases; Neoplasms
|
0.700 |
1.000 |
1 |
2018 |
2018 |
rs9841504
|
0.827 |
0.120 |
3 |
114643917 |
intron variant |
C/G;T
|
snv
|
|
|
Malignant neoplasm of stomach
|
Digestive System Diseases; Neoplasms
|
0.720 |
0.667 |
3 |
2011 |
2016 |
rs10511330
|
0.776 |
0.080 |
3 |
114402172 |
intron variant |
T/C
|
snv
|
|
0.22
|
Malignant tumor of colon
|
Digestive System Diseases; Neoplasms
|
0.700 |
1.000 |
1 |
2018 |
2018 |
rs1560092224
|
0.925 |
0.040 |
3 |
114339276 |
missense variant |
T/A
|
snv
|
|
|
Moderate global developmental delay
|
|
0.700 |
|
0 |
|
|
rs1553794464
|
1.000 |
|
3 |
114350821 |
frameshift variant |
-/C
|
delins
|
|
|
Overgrowth
|
|
0.700 |
1.000 |
7 |
2009 |
2017 |
rs1064795382
|
1.000 |
0.280 |
3 |
114339358 |
missense variant |
T/C
|
snv
|
|
|
Primrose syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders; Otorhinolaryngologic Diseases; Behavior and Behavior Mechanisms
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs483353064
|
1.000 |
0.280 |
3 |
114350310 |
missense variant |
T/G
|
snv
|
|
|
Primrose syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders; Otorhinolaryngologic Diseases; Behavior and Behavior Mechanisms
|
0.800 |
1.000 |
1 |
2014 |
2014 |
rs483353066
|
1.000 |
0.280 |
3 |
114350291 |
missense variant |
T/C
|
snv
|
|
|
Primrose syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders; Otorhinolaryngologic Diseases; Behavior and Behavior Mechanisms
|
0.800 |
1.000 |
1 |
2014 |
2014 |
rs483353068
|
1.000 |
0.280 |
3 |
114339426 |
missense variant |
C/G
|
snv
|
|
|
Primrose syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders; Otorhinolaryngologic Diseases; Behavior and Behavior Mechanisms
|
0.800 |
1.000 |
1 |
2014 |
2014 |
rs483353070
|
1.000 |
0.280 |
3 |
114339370 |
missense variant |
G/A
|
snv
|
|
|
Primrose syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders; Otorhinolaryngologic Diseases; Behavior and Behavior Mechanisms
|
0.800 |
1.000 |
1 |
2014 |
2014 |
rs1057519435
|
1.000 |
0.280 |
3 |
114350292 |
missense variant |
G/A
|
snv
|
|
|
Primrose syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders; Otorhinolaryngologic Diseases; Behavior and Behavior Mechanisms
|
0.700 |
|
0 |
|
|
rs1560110565
|
1.000 |
0.280 |
3 |
114350278 |
missense variant |
G/C
|
snv
|
|
|
Primrose syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders; Otorhinolaryngologic Diseases; Behavior and Behavior Mechanisms
|
0.700 |
|
0 |
|
|
rs483353063
|
1.000 |
0.280 |
3 |
114339355 |
missense variant |
C/T
|
snv
|
|
|
Primrose syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders; Otorhinolaryngologic Diseases; Behavior and Behavior Mechanisms
|
0.700 |
|
0 |
|
|
rs483353065
|
1.000 |
0.280 |
3 |
114350307 |
missense variant |
G/C
|
snv
|
|
|
Primrose syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders; Otorhinolaryngologic Diseases; Behavior and Behavior Mechanisms
|
0.700 |
|
0 |
|
|
rs483353067
|
1.000 |
0.280 |
3 |
114350276 |
missense variant |
G/A;T
|
snv
|
|
|
Primrose syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders; Otorhinolaryngologic Diseases; Behavior and Behavior Mechanisms
|
0.700 |
|
0 |
|
|
rs483353069
|
1.000 |
0.280 |
3 |
114339420 |
missense variant |
T/G
|
snv
|
|
|
Primrose syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders; Otorhinolaryngologic Diseases; Behavior and Behavior Mechanisms
|
0.700 |
|
0 |
|
|
rs9841504
|
0.827 |
0.120 |
3 |
114643917 |
intron variant |
C/G;T
|
snv
|
|
|
Schizophrenia
|
Mental Disorders
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs7647708
|
|
|
3 |
114463586 |
intron variant |
G/A;T
|
snv
|
|
|
Serum albumin measurement
|
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs6438208
|
|
|
3 |
114451425 |
intron variant |
G/A
|
snv
|
|
0.37
|
Smoking
|
Behavior and Behavior Mechanisms
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs9841504
|
0.827 |
0.120 |
3 |
114643917 |
intron variant |
C/G;T
|
snv
|
|
|
Stomach Carcinoma
|
Digestive System Diseases; Neoplasms
|
0.720 |
0.667 |
3 |
2011 |
2016 |
rs1882289
|
|
|
3 |
114742361 |
intron variant |
G/A
|
snv
|
|
0.81
|
Systolic Pressure
|
|
0.700 |
1.000 |
1 |
2018 |
2018 |