rs79184941, FGFR2

N. diseases: 41
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.
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 0.010 1.000 1 2011 2011
Amblyopia
CUI: C0002418
Disease: Amblyopia
29 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 0.010 1.000 1 2006 2006
Astigmatism
CUI: C0004106
Disease: Astigmatism
45 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 0.010 1.000 1 2006 2006
Blepharoptosis
CUI: C0005745
Disease: Blepharoptosis
57 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 0.010 1.000 1 2006 2006
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 0.010 1.000 1 2004 2004
Global developmental delay
CUI: C0557874
Disease: Global developmental delay
553 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 0.010 1.000 1 2014 2014
Muenke Syndrome
CUI: C1864436
Disease: Muenke Syndrome
11 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 0.010 1.000 1 2010 2010
Myopia
CUI: C0027092
Disease: Myopia
167 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 0.010 1.000 1 2006 2006
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 0.010 1.000 1 2007 2007
Osteosarcoma
CUI: C0029463
Disease: Osteosarcoma
178 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 0.010 1.000 1 2004 2004
Osteosarcoma of bone
CUI: C0585442
Disease: Osteosarcoma of bone
151 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 0.010 1.000 1 2004 2004
Ptosis
CUI: C0033377
Disease: Ptosis
12 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 0.010 1.000 1 2006 2006
Ramer Ladda syndrome
CUI: C2930865
Disease: Ramer Ladda syndrome
2 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 0.010 1.000 1 2003 2003
Sagittal craniosynostosis
CUI: C0432123
Disease: Sagittal craniosynostosis
13 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 0.010 1.000 1 2010 2010
Scaphycephaly
CUI: C0265534
Disease: Scaphycephaly
8 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 0.010 1.000 1 2010 2010
Strabismus
CUI: C0038379
Disease: Strabismus
89 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 0.010 1.000 1 2006 2006