rs574034197
|
0.925 |
0.120 |
16 |
89746848 |
missense variant |
T/C;G
|
snv
|
8.7E-05
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
17 |
1997 |
2015 |
rs753063086
|
0.925 |
0.120 |
16 |
89749806 |
missense variant |
G/A;T
|
snv
|
2.0E-05;
1.2E-05
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.800 |
1.000 |
17 |
1997 |
2017 |
rs878853665
|
1.000 |
0.120 |
16 |
89740024 |
missense variant |
A/G
|
snv
|
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
11 |
1997 |
2009 |
rs1429943036
|
1.000 |
0.120 |
16 |
89749805 |
missense variant |
C/A;T
|
snv
|
4.0E-06
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
9 |
1997 |
2008 |
rs1555533300
|
1.000 |
0.120 |
16 |
89739220 |
missense variant |
C/T
|
snv
|
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
9 |
1997 |
2008 |
rs1555533313
|
1.000 |
0.120 |
16 |
89739225 |
missense variant |
C/A
|
snv
|
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
9 |
1997 |
2008 |
rs1555534579
|
1.000 |
0.120 |
16 |
89740848 |
missense variant |
A/G
|
snv
|
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
9 |
1997 |
2008 |
rs374030577
|
1.000 |
0.120 |
16 |
89767215 |
missense variant |
A/C;T
|
snv
|
4.0E-06
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
9 |
1997 |
2008 |
rs76275444
|
1.000 |
0.120 |
16 |
89816592 |
missense variant |
G/A;C
|
snv
|
5.0E-03
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
9 |
1997 |
2008 |
rs755546887
|
0.925 |
0.120 |
16 |
89761950 |
missense variant |
G/A;T
|
snv
|
2.4E-05;
4.0E-06
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
7 |
2005 |
2016 |
rs759877008
|
0.925 |
0.120 |
16 |
89805275 |
splice region variant |
C/A;T
|
snv
|
1.6E-05
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
7 |
1999 |
2018 |
rs755922289
|
0.925 |
0.120 |
16 |
89761949 |
missense variant |
C/A;T
|
snv
|
5.2E-05
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
6 |
2000 |
2015 |
rs776969626
|
1.000 |
0.120 |
16 |
89739175 |
frameshift variant |
TG/-
|
delins
|
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
5 |
2011 |
2016 |
rs1490352414
|
1.000 |
0.120 |
16 |
89770179 |
missense variant |
A/G
|
snv
|
9.5E-06
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
4 |
2005 |
2012 |
rs752160950
|
0.925 |
0.120 |
16 |
89767185 |
stop gained |
G/A;C
|
snv
|
1.2E-05;
4.0E-06
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
4 |
2005 |
2015 |
rs762526878
|
1.000 |
0.120 |
16 |
89771778 |
missense variant |
A/G
|
snv
|
8.0E-06
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
4 |
2005 |
2014 |
rs769479800
|
0.925 |
0.120 |
16 |
89816614 |
start lost |
A/G;T
|
snv
|
4.1E-05;
8.3E-06
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
4 |
2005 |
2014 |
rs1555538571
|
1.000 |
0.120 |
16 |
89749730 |
missense variant |
C/T
|
snv
|
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
3 |
2005 |
2014 |
rs1555545592
|
1.000 |
0.120 |
16 |
89765068 |
splice acceptor variant |
T/A
|
snv
|
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
3 |
1999 |
2013 |
rs1555580427
|
1.000 |
0.120 |
16 |
89815903 |
stop gained |
G/A
|
snv
|
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
3 |
1999 |
2016 |
rs751266148
|
1.000 |
0.120 |
16 |
89748658 |
splice donor variant |
C/A;T
|
snv
|
4.0E-06
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
3 |
2013 |
2016 |
rs915983602
|
1.000 |
0.120 |
16 |
89738710 |
splice acceptor variant |
T/A;C;G
|
snv
|
4.0E-06;
4.0E-06;
4.0E-06
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
3 |
2004 |
2016 |
rs927630499
|
1.000 |
0.120 |
16 |
89758688 |
stop gained |
C/T
|
snv
|
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
3 |
2008 |
2013 |
rs1247378731
|
1.000 |
0.120 |
16 |
89767213 |
stop gained |
G/A;C;T
|
snv
|
4.0E-06;
1.2E-05;
4.0E-06
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
2 |
2005 |
2005 |
rs1285346388
|
1.000 |
0.120 |
16 |
89758702 |
splice acceptor variant |
CTAGAACAGCAAACACTGC/-
|
delins
|
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
2 |
1997 |
2008 |