Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs137852985
rs137852985
1.000 0.080 17 61808488 missense variant C/T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 7 2001 2014
dbSNP: rs587778134
rs587778134
0.851 0.320 17 61776459 frameshift variant AA/-;AAAA delins
FANCONI ANEMIA, COMPLEMENTATION GROUP J
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.700 1.000 6 2011 2016
dbSNP: rs587780833
rs587780833
0.925 0.200 17 61847100 splice donor variant C/T snv
FANCONI ANEMIA, COMPLEMENTATION GROUP J
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.700 1.000 5 2005 2016
dbSNP: rs587780833
rs587780833
0.925 0.200 17 61847100 splice donor variant C/T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 5 2005 2016
dbSNP: rs587782047
rs587782047
0.925 0.200 17 61861446 splice donor variant C/A;T snv
FANCONI ANEMIA, COMPLEMENTATION GROUP J
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.700 1.000 5 2005 2016
dbSNP: rs1295703239
rs1295703239
0.925 0.200 17 61685952 frameshift variant AGAT/-;AGATAGAT delins 7.0E-06
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 4 2008 2011
dbSNP: rs1295703239
rs1295703239
0.925 0.200 17 61685952 frameshift variant AGAT/-;AGATAGAT delins 7.0E-06
FANCONI ANEMIA, COMPLEMENTATION GROUP J
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.700 1.000 4 2008 2011
dbSNP: rs1555573327
rs1555573327
0.925 0.200 17 61685949 frameshift variant G/- delins
FANCONI ANEMIA, COMPLEMENTATION GROUP J
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.700 1.000 4 2008 2011
dbSNP: rs1555573327
rs1555573327
0.925 0.200 17 61685949 frameshift variant G/- delins
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 4 2008 2011
dbSNP: rs587778134
rs587778134
0.851 0.320 17 61776459 frameshift variant AA/-;AAAA delins
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.700 1.000 4 2015 2016
dbSNP: rs771028677
rs771028677
0.882 0.280 17 61684053 frameshift variant TGTT/-;TGTTTGTT delins 2.1E-05
FANCONI ANEMIA, COMPLEMENTATION GROUP J
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.700 1.000 4 2008 2016
dbSNP: rs786202927
rs786202927
17 61683814 stop gained T/A snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms 0.700 1.000 4 2010 2012
dbSNP: rs864622277
rs864622277
0.925 0.240 17 61847221 splice acceptor variant C/G snv
FANCONI ANEMIA, COMPLEMENTATION GROUP J
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.700 1.000 4 2005 2016
dbSNP: rs869312763
rs869312763
0.925 0.200 17 61686167 splice acceptor variant T/C snv
FANCONI ANEMIA, COMPLEMENTATION GROUP J
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.700 1.000 4 2005 2016
dbSNP: rs1057519365
rs1057519365
0.851 0.320 17 61780931 frameshift variant TT/- delins
FANCONI ANEMIA, COMPLEMENTATION GROUP J
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.700 1.000 3 2011 2016
dbSNP: rs1057519365
rs1057519365
0.851 0.320 17 61780931 frameshift variant TT/- delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms 0.700 1.000 3 2011 2016
dbSNP: rs1064793887
rs1064793887
0.925 0.240 17 61743135 splice acceptor variant C/T snv
FANCONI ANEMIA, COMPLEMENTATION GROUP J
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.700 1.000 3 2005 2011
dbSNP: rs1555607022
rs1555607022
0.925 0.200 17 61799099 splice donor variant C/T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 3 2005 2011
dbSNP: rs1555607022
rs1555607022
0.925 0.200 17 61799099 splice donor variant C/T snv
FANCONI ANEMIA, COMPLEMENTATION GROUP J
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.700 1.000 3 2005 2011
dbSNP: rs1555607628
rs1555607628
0.925 0.200 17 61801252 splice donor variant C/T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 3 2005 2011
dbSNP: rs1555607628
rs1555607628
0.925 0.200 17 61801252 splice donor variant C/T snv
FANCONI ANEMIA, COMPLEMENTATION GROUP J
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.700 1.000 3 2005 2011
dbSNP: rs1555617934
rs1555617934
1.000 0.120 17 61857232 splice acceptor variant C/A snv
FANCONI ANEMIA, COMPLEMENTATION GROUP J
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.700 1.000 3 2005 2011
dbSNP: rs1567756032
rs1567756032
1.000 0.120 17 61716064 splice acceptor variant C/T snv
FANCONI ANEMIA, COMPLEMENTATION GROUP J
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.700 1.000 3 2005 2011
dbSNP: rs587782047
rs587782047
0.925 0.200 17 61861446 splice donor variant C/A;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 3 2005 2011
dbSNP: rs587782539
rs587782539
0.925 0.200 17 61686166 splice acceptor variant C/T snv
FANCONI ANEMIA, COMPLEMENTATION GROUP J
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.700 1.000 3 2005 2011