rs863225281, ALK

N. diseases: 12
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
NEUROBLASTOMA, SUSCEPTIBILITY TO, 3
CUI: C2751681
Disease: NEUROBLASTOMA, SUSCEPTIBILITY TO, 3
16 0.776 0.200 2 29220829 missense variant G/C;T snv 0.800 0
NEUROBLASTOMA, SUSCEPTIBILITY TO
CUI: C2749484
Disease: NEUROBLASTOMA, SUSCEPTIBILITY TO
34 0.776 0.200 2 29220829 missense variant G/C;T snv 0.700 1.000 6 2008 2016
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.776 0.200 2 29220829 missense variant G/C;T snv 0.700 1.000 2 2012 2014
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.776 0.200 2 29220829 missense variant G/C;T snv 0.100 1.000 15 2008 2019
Childhood Neuroblastoma
CUI: C4086165
Disease: Childhood Neuroblastoma
231 0.776 0.200 2 29220829 missense variant G/C;T snv 0.100 1.000 15 2008 2019
Neuroblastoma
CUI: C0027819
Disease: Neuroblastoma
386 0.776 0.200 2 29220829 missense variant G/C;T snv 0.100 1.000 15 2008 2019
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.776 0.200 2 29220829 missense variant G/C;T snv 0.080 1.000 8 2010 2016
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.776 0.200 2 29220829 missense variant G/C;T snv 0.020 1.000 2 2014 2019
Congenital chromosomal disease
CUI: C0008626
Disease: Congenital chromosomal disease
47 0.776 0.200 2 29220829 missense variant G/C;T snv 0.010 1.000 1 2012 2012
hereditary neuroblastoma
CUI: C3899155
Disease: hereditary neuroblastoma
4 0.776 0.200 2 29220829 missense variant G/C;T snv 0.010 1.000 1 2017 2017
Inflammatory Myofibroblastic Tumor
CUI: C0334121
Disease: Inflammatory Myofibroblastic Tumor
2 0.776 0.200 2 29220829 missense variant G/C;T snv 0.010 1.000 1 2010 2010
Neuroblastoma recurrent
CUI: C0278695
Disease: Neuroblastoma recurrent
2 0.776 0.200 2 29220829 missense variant G/C;T snv 0.010 1.000 1 2019 2019