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: rs17483466
rs17483466
ACOXL ; MIR4435-2HG
0.827 0.280 2 111039881 intron variant A/G snv 0.15
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.830 1.000 3 2008 2013
dbSNP: rs17483466
rs17483466
ACOXL ; MIR4435-2HG
0.827 0.280 2 111039881 intron variant A/G snv 0.15
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma 		0.700 1.000 3 2008 2013
dbSNP: rs6720394
rs6720394
MIR4435-2HG
0.925 0.040 2 111231795 intron variant T/G snv 0.11
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2011 2011
dbSNP: rs6738028
rs6738028
MIR4435-2HG
2 111191750 intron variant G/C snv 0.64
CUI: C0441683
Disease: Hormone measurement
Hormone measurement 		0.800 1.000 1 2011 2011
dbSNP: rs7578982
rs7578982
ACOXL ; MIR4435-2HG
2 111078961 intron variant T/C snv 0.27
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs7578982
rs7578982
ACOXL ; MIR4435-2HG
2 111078961 intron variant T/C snv 0.27
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2011 2011
dbSNP: rs10207392
rs10207392
ACOXL ; MIR4435-2HG
2 111092082 intron variant A/G snv 0.48
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2012 2012
dbSNP: rs2271404
rs2271404
MIR4435-2HG
1.000 0.120 2 111246290 non coding transcript exon variant T/C snv 0.12
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		0.800 1.000 1 2012 2012
dbSNP: rs1439287
rs1439287
ACOXL ; ACOXL-AS1 ; MIR4435-2HG
0.925 0.120 2 111114320 non coding transcript exon variant G/A snv 0.42
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.800 1.000 1 2014 2014
dbSNP: rs1439287
rs1439287
ACOXL ; ACOXL-AS1 ; MIR4435-2HG
0.925 0.120 2 111114320 non coding transcript exon variant G/A snv 0.42
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma 		0.700 1.000 1 2014 2014
dbSNP: rs58055674
rs58055674
ACOXL ; MIR4435-2HG
0.925 0.120 2 111074216 intron variant T/C snv 0.13
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.700 1.000 2 2016 2017
dbSNP: rs58055674
rs58055674
ACOXL ; MIR4435-2HG
0.925 0.120 2 111074216 intron variant T/C snv 0.13
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma 		0.700 1.000 2 2016 2017
dbSNP: rs62160676
rs62160676
MIR4435-2HG
2 111410354 intron variant T/C;G snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 2 2016 2019
dbSNP: rs62160676
rs62160676
MIR4435-2HG
2 111410354 intron variant T/C;G snv
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 2 2016 2019
dbSNP: rs112744032
rs112744032
MIR4435-2HG ; SOCAR
2 111521757 intron variant G/- delins
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs113993396
rs113993396
MIR4435-2HG
2 111359727 intron variant C/G snv 5.9E-02
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs138308793
rs138308793
MIR4435-2HG ; SOCAR
2 111493181 intron variant G/A snv 0.11
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs143800403
rs143800403
MIR4435-2HG
2 111373568 intron variant C/A;T snv
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs1448203
rs1448203
MIR4435-2HG ; SOCAR
2 111510708 non coding transcript exon variant T/A;C snv
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs150784178
rs150784178
ACOXL ; ACOXL-AS1 ; MIR4435-2HG
2 111116484 intron variant CTCTGAAAACCTGAAATG/- delins 0.11
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs17484848
rs17484848
BCL2L11 ; MIR4435-2HG
2 111142983 intron variant T/C snv 7.2E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs17484848
rs17484848
BCL2L11 ; MIR4435-2HG
2 111142983 intron variant T/C snv 7.2E-02
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs2334232
rs2334232
MIR4435-2HG
2 111371516 intron variant G/A snv 0.18
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs3789088
rs3789088
ACOXL ; MIR4435-2HG
2 111033227 intron variant G/C snv 0.14
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs3789088
rs3789088
ACOXL ; MIR4435-2HG
2 111033227 intron variant G/C snv 0.14
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2016 2016