LGALS3, galectin 3, 3958

N. diseases: 557; N. variants: 15
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: rs1009977
rs1009977 		1.000 0.040 14 55136284 intron variant T/G snv 0.48
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1009978
rs1009978 		14 55136343 intron variant C/G;T snv
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10498475
rs10498475 		14 55145762 downstream gene variant C/T snv 5.7E-02
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2075601
rs2075601 		14 55142516 intron variant C/T snv 0.57
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2075602
rs2075602 		14 55143056 intron variant A/G;T snv
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2075603
rs2075603 		14 55143237 intron variant C/A snv 0.36
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs3825613
rs3825613 		14 55126454 intron variant A/C snv 0.36
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4644
rs4644 		0.732 0.320 14 55138217 missense variant C/A;G snv 0.35
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4652
rs4652 		0.752 0.200 14 55138318 missense variant A/C snv 4.1E-06; 0.45 0.57
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs76426991
rs76426991 		14 55134221 intron variant G/A snv 5.7E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs8004787
rs8004787 		14 55140648 intron variant C/T snv 0.57
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs8013027
rs8013027 		14 55144222 intron variant C/G snv 0.42
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1009977
rs1009977 		1.000 0.040 14 55136284 intron variant T/G snv 0.48
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic 		Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs11125
rs11125 		0.851 0.120 14 55145121 missense variant A/T snv 6.5E-02 5.7E-02
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2017 2017
dbSNP: rs11125
rs11125 		0.851 0.120 14 55145121 missense variant A/T snv 6.5E-02 5.7E-02
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2017 2017
dbSNP: rs11125
rs11125 		0.851 0.120 14 55145121 missense variant A/T snv 6.5E-02 5.7E-02
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs11125
rs11125 		0.851 0.120 14 55145121 missense variant A/T snv 6.5E-02 5.7E-02
CUI: C4048328
Disease: cervical cancer
cervical cancer 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2017 2017
dbSNP: rs11125
rs11125 		0.851 0.120 14 55145121 missense variant A/T snv 6.5E-02 5.7E-02
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
Secondary malignant neoplasm of lymph node 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs4644
rs4644 		0.732 0.320 14 55138217 missense variant C/A;G snv 0.35
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2008 2008
dbSNP: rs4644
rs4644 		0.732 0.320 14 55138217 missense variant C/A;G snv 0.35
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2013 2013
dbSNP: rs4644
rs4644 		0.732 0.320 14 55138217 missense variant C/A;G snv 0.35
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia 		Nutritional and Metabolic Diseases 0.010 1.000 1 2016 2016
dbSNP: rs4644
rs4644 		0.732 0.320 14 55138217 missense variant C/A;G snv 0.35
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs4644
rs4644 		0.732 0.320 14 55138217 missense variant C/A;G snv 0.35
CUI: C0278878
Disease: Adult Glioblastoma
Adult Glioblastoma 		Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs4644
rs4644 		0.732 0.320 14 55138217 missense variant C/A;G snv 0.35
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2013 2013
dbSNP: rs4644
rs4644 		0.732 0.320 14 55138217 missense variant C/A;G snv 0.35
CUI: C3853962
Disease: Enterovirus 71 infection
Enterovirus 71 infection 		Infections 0.010 1.000 1 2016 2016