FGFR3, fibroblast growth factor receptor 3, 2261

N. diseases: 654; N. variants: 55
Disease: Carcinoma ×
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: rs121913483
rs121913483 		0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05
CUI: C0007097
Disease: Carcinoma
Carcinoma 		Neoplasms 0.740 1.000 5 1999 2005
dbSNP: rs78311289
rs78311289 		0.689 0.440 4 1806162 missense variant A/C;G snv 4.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma 		Neoplasms 0.710 1.000 3 1999 2001
dbSNP: rs121913480
rs121913480 		1.000 0.120 4 1806604 missense variant G/T snv
CUI: C0007097
Disease: Carcinoma
Carcinoma 		Neoplasms 0.700 1.000 1 2005 2005
dbSNP: rs121913482
rs121913482 		0.630 0.680 4 1801837 missense variant C/T snv
CUI: C0007097
Disease: Carcinoma
Carcinoma 		Neoplasms 0.700 1.000 1 1999 1999
dbSNP: rs121913484
rs121913484 		0.851 0.240 4 1804365 missense variant A/T snv
CUI: C0007097
Disease: Carcinoma
Carcinoma 		Neoplasms 0.700 1.000 1 2002 2002
dbSNP: rs121913485
rs121913485 		0.716 0.400 4 1804372 missense variant A/G snv
CUI: C0007097
Disease: Carcinoma
Carcinoma 		Neoplasms 0.700 1.000 1 2001 2001
dbSNP: rs28931615
rs28931615 		0.732 0.240 4 1804426 missense variant C/A;T snv
CUI: C0007097
Disease: Carcinoma
Carcinoma 		Neoplasms 0.700 1.000 1 2009 2009
dbSNP: rs587779383
rs587779383 		0.851 0.120 4 1806157 missense variant A/C;G;T snv
CUI: C0007097
Disease: Carcinoma
Carcinoma 		Neoplasms 0.700 1.000 1 1998 1998