SLC23A2, solute carrier family 23 member 2, 9962

N. diseases: 46; N. variants: 10
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: rs1279682
rs1279682 		20 4999759 intron variant C/T snv 0.20
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs1279682
rs1279682 		20 4999759 intron variant C/T snv 0.20
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs1279683
rs1279683 		1.000 0.040 20 5002446 intron variant G/A;C snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1279683
rs1279683 		1.000 0.040 20 5002446 intron variant G/A;C snv
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs6053022
rs6053022 		1.000 0.040 20 4992810 intron variant A/G snv 0.36
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		Mental Disorders 0.700 1.000 1 2012 2012
dbSNP: rs1279683
rs1279683 		1.000 0.040 20 5002446 intron variant G/A;C snv
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle 		Eye Diseases 0.020 1.000 2 2011 2013
dbSNP: rs1110277
rs1110277 		0.925 0.080 20 4874036 synonymous variant A/G snv 0.34 0.43
CUI: C0023530
Disease: Leukopenia
Leukopenia 		Hemic and Lymphatic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1110277
rs1110277 		0.925 0.080 20 4874036 synonymous variant A/G snv 0.34 0.43
CUI: C0038362
Disease: Stomatitis
Stomatitis 		Stomatognathic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs12479919
rs12479919 		0.925 0.080 20 5000094 intron variant C/T snv 0.32
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2009 2009
dbSNP: rs12479919
rs12479919 		0.925 0.080 20 5000094 intron variant C/T snv 0.32
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2009 2009
dbSNP: rs1776948
rs1776948 		1.000 0.120 20 4950467 intron variant G/A;C snv
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1776964
rs1776964 		1.000 0.040 20 4899662 synonymous variant G/A snv 0.47 0.45
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome 		Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs4987219
rs4987219 		0.925 0.080 20 4884300 intron variant C/G;T snv
CUI: C0038362
Disease: Stomatitis
Stomatitis 		Stomatognathic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs4987219
rs4987219 		0.925 0.080 20 4884300 intron variant C/G;T snv
CUI: C0023530
Disease: Leukopenia
Leukopenia 		Hemic and Lymphatic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs6133175
rs6133175 		1.000 0.120 20 4911113 intron variant A/G snv 0.28
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs6139591
rs6139591 		1.000 0.040 20 4970713 intron variant G/A snv 0.40
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome 		Cardiovascular Diseases 0.010 1.000 1 2013 2013