Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs17607589
rs17607589
LPP
3 188684798 intron variant C/T snv 0.13
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2017 2017
dbSNP: rs17670280
rs17670280
LPP
1.000 0.080 3 188682451 intron variant G/A;C snv
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs17670280
rs17670280
LPP
1.000 0.080 3 188682451 intron variant G/A;C snv
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
dbSNP: rs191177147
rs191177147
LPP
0.882 0.040 3 188374758 intron variant G/T snv
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.700 1.000 1 2016 2016
dbSNP: rs191177147
rs191177147
LPP
0.882 0.040 3 188374758 intron variant G/T snv
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs191177147
rs191177147
LPP
0.882 0.040 3 188374758 intron variant G/T snv
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.700 1.000 1 2016 2016
dbSNP: rs2030519
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2016 2016
dbSNP: rs2030519
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs2030519
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		0.700 1.000 1 2018 2018
dbSNP: rs2030519
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2019 2019
dbSNP: rs2030519
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2019 2019
dbSNP: rs2030519
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2019 2019
dbSNP: rs2030520
rs2030520
LPP
3 188401794 intron variant C/G;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs2889896
rs2889896
LPP
1.000 0.080 3 188384928 intron variant C/T snv 0.43
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
dbSNP: rs3856920
rs3856920
LPP
3 188823038 intron variant A/G snv 0.25
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4132172
rs4132172
LPP
3 188343926 intron variant C/T snv 0.32
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs4420855
rs4420855
LPP
3 188339419 intron variant A/G snv 0.43
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs4459895
rs4459895
LPP
0.827 0.160 3 188236626 intron variant A/C snv 0.88
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma 		0.700 1.000 1 2017 2017
dbSNP: rs4459895
rs4459895
LPP
0.827 0.160 3 188236626 intron variant A/C snv 0.88
CUI: C0152268
Disease: Nodular Sclerosis Classical Hodgkin Lymphoma
Nodular Sclerosis Classical Hodgkin Lymphoma 		0.700 1.000 1 2017 2017
dbSNP: rs4459895
rs4459895
LPP
0.827 0.160 3 188236626 intron variant A/C snv 0.88
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		0.700 1.000 1 2017 2017
dbSNP: rs4459895
rs4459895
LPP
0.827 0.160 3 188236626 intron variant A/C snv 0.88
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.700 1.000 1 2017 2017
dbSNP: rs4686952
rs4686952
LPP
3 188331054 intron variant G/A snv 0.43
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4686991
rs4686991
LPP
3 188647490 intron variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs542618547
rs542618547
LPP
3 188728876 intron variant AAA/-;A;AA;AAAA;AAAAA delins 0.23
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs542618547
rs542618547
LPP
3 188728876 intron variant AAA/-;A;AA;AAAA;AAAAA delins 0.23
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016