FCRL3, Fc receptor like 3, 115352

N. diseases: 62; N. variants: 13
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: rs3761959
rs3761959 		0.827 0.320 1 157699488 intron variant C/A;G;T snv
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.810 1.000 2 2011 2013
dbSNP: rs7528684
rs7528684 		0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement 		0.800 1.000 1 2011 2011
dbSNP: rs11264799
rs11264799 		0.851 0.240 1 157700967 upstream gene variant C/T snv 0.28
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases 0.720 1.000 3 2015 2020
dbSNP: rs3761959
rs3761959 		0.827 0.320 1 157699488 intron variant C/A;G;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.710 1.000 2 2006 2015
dbSNP: rs3761959
rs3761959 		0.827 0.320 1 157699488 intron variant C/A;G;T snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.710 1.000 2 2016 2016
dbSNP: rs11264794
rs11264794 		1.000 0.120 1 157677999 3 prime UTR variant C/A snv 0.63
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs2210913
rs2210913 		0.925 0.080 1 157699203 intron variant C/T snv 0.56
CUI: C0162538
Disease: Immunoglobulin A deficiency (disorder)
Immunoglobulin A deficiency (disorder) 		Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2016 2016
dbSNP: rs2210913
rs2210913 		0.925 0.080 1 157699203 intron variant C/T snv 0.56
CUI: C4049006
Disease: Selective immunoglobulin A deficiency
Selective immunoglobulin A deficiency 		0.700 1.000 1 2016 2016
dbSNP: rs3761959
rs3761959 		0.827 0.320 1 157699488 intron variant C/A;G;T snv
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2016 2016
dbSNP: rs7522061
rs7522061 		0.882 0.320 1 157698600 missense variant T/C;G snv 0.45 0.51
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7522061
rs7522061 		0.882 0.320 1 157698600 missense variant T/C;G snv 0.45 0.51
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs7528684
rs7528684 		0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs7528684
rs7528684 		0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7528684
rs7528684 		0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.050 1.000 5 2006 2016
dbSNP: rs11264794
rs11264794 		1.000 0.120 1 157677999 3 prime UTR variant C/A snv 0.63
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases 0.020 1.000 2 2019 2020
dbSNP: rs7528684
rs7528684 		0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57
CUI: C0014175
Disease: Endometriosis
Endometriosis 		Female Urogenital Diseases and Pregnancy Complications 0.020 1.000 2 2012 2013
dbSNP: rs7528684
rs7528684 		0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		Immune System Diseases 0.020 1.000 2 2013 2014
dbSNP: rs7528684
rs7528684 		0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.020 1.000 2 2010 2013
dbSNP: rs7528684
rs7528684 		0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.020 1.000 2 2013 2014
dbSNP: rs10489678
rs10489678 		1.000 0.120 1 157699878 intron variant G/A;C;T snv
CUI: C4275242
Disease: Sudden sensorineural hearing loss
Sudden sensorineural hearing loss 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs11264793
rs11264793 		1.000 0.120 1 157677736 3 prime UTR variant A/T snv 0.28
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases 0.010 1.000 1 2020 2020
dbSNP: rs11264799
rs11264799 		0.851 0.240 1 157700967 upstream gene variant C/T snv 0.28
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		Immune System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs11264799
rs11264799 		0.851 0.240 1 157700967 upstream gene variant C/T snv 0.28
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.010 1.000 1 2006 2006
dbSNP: rs11264799
rs11264799 		0.851 0.240 1 157700967 upstream gene variant C/T snv 0.28
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs11264799
rs11264799 		0.851 0.240 1 157700967 upstream gene variant C/T snv 0.28
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.010 1.000 1 2007 2007