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: 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
dbSNP: rs3789087
rs3789087
ACOXL ; MIR4435-2HG
2 111034076 intron variant C/T snv 0.14
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2018 2018
dbSNP: rs3789087
rs3789087
ACOXL ; MIR4435-2HG
2 111034076 intron variant C/T snv 0.14
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2018 2018
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: rs116008367
rs116008367
ACOXL ; MIR4435-2HG
2 111049969 intron variant G/C snv 5.0E-03
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs2009581
rs2009581
ACOXL ; MIR4435-2HG
2 111050100 intron variant G/A snv 0.26
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: rs2009581
rs2009581
ACOXL ; MIR4435-2HG
2 111050100 intron variant G/A snv 0.26
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs2009581
rs2009581
ACOXL ; MIR4435-2HG
2 111050100 intron variant G/A snv 0.26
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs2880119
rs2880119
ACOXL ; MIR4435-2HG
2 111051753 intron variant C/A;T snv
CUI: C0730345
Disease: Microalbuminuria
Microalbuminuria 		0.700 1.000 1 2019 2019
dbSNP: rs4848370
rs4848370
ACOXL ; MIR4435-2HG
2 111054088 intron variant C/T snv 0.25
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs4848370
rs4848370
ACOXL ; MIR4435-2HG
2 111054088 intron variant C/T snv 0.25
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs2165109
rs2165109
ACOXL ; MIR4435-2HG
0.925 0.120 2 111061081 intron variant A/C snv 0.25
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		0.700 1.000 1 2017 2017
dbSNP: rs2165109
rs2165109
ACOXL ; MIR4435-2HG
0.925 0.120 2 111061081 intron variant A/C snv 0.25
CUI: C1335177
Disease: Ovarian Serous Adenocarcinoma
Ovarian Serous Adenocarcinoma 		0.700 1.000 1 2017 2017
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: rs34931195
rs34931195
ACOXL ; MIR4435-2HG
2 111074488 intron variant T/A snv 0.27
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
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: rs12711846
rs12711846
ACOXL ; ACOXL-AS1 ; MIR4435-2HG
0.851 0.160 2 111098716 non coding transcript exon variant A/G snv 0.26
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma 		0.700 1.000 1 2017 2017
dbSNP: rs12711846
rs12711846
ACOXL ; ACOXL-AS1 ; MIR4435-2HG
0.851 0.160 2 111098716 non coding transcript exon variant A/G snv 0.26
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.700 1.000 1 2017 2017
dbSNP: rs12711846
rs12711846
ACOXL ; ACOXL-AS1 ; MIR4435-2HG
0.851 0.160 2 111098716 non coding transcript exon variant A/G snv 0.26
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		0.700 1.000 1 2017 2017
dbSNP: rs12711846
rs12711846
ACOXL ; ACOXL-AS1 ; MIR4435-2HG
0.851 0.160 2 111098716 non coding transcript exon variant A/G snv 0.26
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		0.700 1.000 1 2017 2017