rs121918324
|
0.925 |
0.160 |
1 |
161167187 |
missense variant |
C/T
|
snv
|
|
|
Variegate Porphyria
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.880 |
1.000 |
25 |
1996 |
2013 |
rs121918323
|
1.000 |
0.160 |
1 |
161169070 |
missense variant |
G/C
|
snv
|
|
|
Variegate Porphyria
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
20 |
1996 |
2013 |
rs121918325
|
1.000 |
0.160 |
1 |
161168462 |
missense variant |
C/T
|
snv
|
4.0E-06
|
|
Variegate Porphyria
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
20 |
1996 |
2013 |
rs121918326
|
1.000 |
0.160 |
1 |
161166906 |
missense variant |
A/C
|
snv
|
|
|
Variegate Porphyria
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
20 |
1996 |
2013 |
rs1361576529
|
1.000 |
0.160 |
1 |
161171039 |
missense variant |
G/C
|
snv
|
|
|
Variegate Porphyria
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
1.000 |
20 |
1996 |
2013 |
rs141274934
|
1.000 |
0.160 |
1 |
161170711 |
missense variant |
C/A;G
|
snv
|
4.0E-06
|
|
Variegate Porphyria
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
1.000 |
20 |
1996 |
2013 |
rs374936130
|
1.000 |
0.160 |
1 |
161170493 |
missense variant |
G/A;C
|
snv
|
8.0E-06
|
|
Variegate Porphyria
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
1.000 |
20 |
1996 |
2013 |
rs757473753
|
1.000 |
0.160 |
1 |
161168492 |
missense variant |
C/G
|
snv
|
4.0E-06
|
7.0E-06
|
Variegate Porphyria
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
1.000 |
20 |
1996 |
2013 |
rs764352037
|
1.000 |
0.160 |
1 |
161167181 |
missense variant |
G/A
|
snv
|
4.0E-06
|
|
Variegate Porphyria
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
1.000 |
20 |
1996 |
2013 |
rs767419411
|
0.882 |
0.200 |
1 |
161168069 |
missense variant |
G/A;C
|
snv
|
1.2E-05;
8.0E-06
|
|
Variegate Porphyria
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
1.000 |
20 |
1996 |
2013 |
rs769452432
|
1.000 |
0.160 |
1 |
161166892 |
missense variant |
G/T
|
snv
|
|
|
Variegate Porphyria
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
1.000 |
20 |
1996 |
2013 |
rs776530007
|
1.000 |
0.160 |
1 |
161170724 |
missense variant |
A/C;T
|
snv
|
4.0E-06;
4.0E-06
|
|
Variegate Porphyria
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
1.000 |
20 |
1996 |
2013 |
rs1558033572
|
1.000 |
0.160 |
1 |
161169903 |
splice acceptor variant |
TA/-
|
del
|
|
|
Variegate Porphyria
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
1.000 |
3 |
1991 |
2001 |
rs2301287
|
|
|
1 |
161167053 |
intron variant |
C/G;T
|
snv
|
0.37;
2.8E-05
|
|
mathematical ability
|
|
0.700 |
1.000 |
1 |
2018 |
2018 |
rs1057518798
|
1.000 |
0.120 |
1 |
161170939 |
stop gained |
G/A
|
snv
|
|
|
Abdominal colic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
0.700 |
|
0 |
|
|
rs1057518798
|
1.000 |
0.120 |
1 |
161170939 |
stop gained |
G/A
|
snv
|
|
|
Abnormal blistering of the skin
|
|
0.700 |
|
0 |
|
|
rs1057518798
|
1.000 |
0.120 |
1 |
161170939 |
stop gained |
G/A
|
snv
|
|
|
Porphyruria
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs1317835140
|
1.000 |
0.160 |
1 |
161167131 |
missense variant |
G/A
|
snv
|
4.0E-06
|
|
Variegate Porphyria
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs148292941
|
|
|
1 |
161171095 |
stop gained |
T/C;G
|
snv
|
8.0E-06
|
6.3E-05
|
Abnormal blistering of the skin
|
|
0.700 |
|
0 |
|
|
rs148292941
|
|
|
1 |
161171095 |
stop gained |
T/C;G
|
snv
|
8.0E-06
|
6.3E-05
|
Urine Discoloration
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.700 |
|
0 |
|
|
rs148292941
|
|
|
1 |
161171095 |
stop gained |
T/C;G
|
snv
|
8.0E-06
|
6.3E-05
|
Constipation
|
Pathological Conditions, Signs and Symptoms
|
0.700 |
|
0 |
|
|
rs148292941
|
|
|
1 |
161171095 |
stop gained |
T/C;G
|
snv
|
8.0E-06
|
6.3E-05
|
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1
|
|
0.700 |
|
0 |
|
|
rs28936676
|
0.925 |
0.160 |
1 |
161170467 |
stop lost |
A/C
|
snv
|
|
|
Homozygous variegate porphyria
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs28936676
|
0.925 |
0.160 |
1 |
161170467 |
stop lost |
A/C
|
snv
|
|
|
Variegate Porphyria
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs28936677
|
1.000 |
0.160 |
1 |
161166882 |
missense variant |
T/C
|
snv
|
2.4E-05
|
4.9E-05
|
Homozygous variegate porphyria
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|