FGFR1OP, FGFR1 oncogene partner, 11116

N. diseases: 40; N. variants: 9
Disease: Graves Disease ×
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: rs12526548
rs12526548 		1.000 0.120 6 167017659 intron variant C/T snv 0.43
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs204295
rs204295 		1.000 0.120 6 167087074 intron variant C/T snv 0.50
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs2301436
rs2301436 		0.752 0.320 6 167024500 intron variant C/T snv 0.42
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs368397331
rs368397331 		1.000 0.120 6 167004623 intron variant A/C snv
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs6902119
rs6902119 		0.882 0.160 6 167092303 intron variant T/C;G snv
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2015 2015