MECOM-AS1, MECOM antisense RNA 1, 105374205

N. diseases: 7; N. variants: 9
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: rs10711289
rs10711289
3 169450583 intron variant AAA/-;A;AA;AAAA;AAAAA delins
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs12632583
rs12632583
1.000 0.040 3 169464399 intron variant A/G snv 4.1E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1343040
rs1343040
3 169468505 intron variant G/A snv 0.36
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs1918973
rs1918973
3 169447385 intron variant A/G snv 0.57
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs1918973
rs1918973
3 169447385 intron variant A/G snv 0.57
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs1918974
rs1918974
1.000 0.040 3 169448100 intron variant C/T snv 0.57
Diastolic blood pressure measurement
0.700 1.000 1 2009 2009
dbSNP: rs1918974
rs1918974
1.000 0.040 3 169448100 intron variant C/T snv 0.57
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs1918974
rs1918974
1.000 0.040 3 169448100 intron variant C/T snv 0.57
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2009 2009
dbSNP: rs1918976
rs1918976
1.000 0.040 3 169466635 intron variant C/T snv 1.5E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs3817581
rs3817581
1.000 0.040 3 169463794 intron variant C/T snv 0.45
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs4955659
rs4955659
1.000 0.040 3 169453830 intron variant A/T snv 4.1E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs73174306
rs73174306
3 169476456 intron variant A/C;G;T snv 2.8E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018