MEF2B, myocyte enhancer factor 2B, 100271849

N. diseases: 42; N. variants: 4
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: rs58190593
rs58190593
19 19153129 intron variant C/T snv 0.16
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 2 2018 2018
dbSNP: rs75746498
rs75746498
19 19149877 intron variant G/A;C;T snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 2 2018 2018
dbSNP: rs11668319
rs11668319
19 19185066 intron variant A/G snv 0.15
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs11668319
rs11668319
19 19185066 intron variant A/G snv 0.15
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs11668319
rs11668319
19 19185066 intron variant A/G snv 0.15
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs58190593
rs58190593
19 19153129 intron variant C/T snv 0.16
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs7360000
rs7360000
19 19156039 intron variant C/T snv 0.18
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs7360000
rs7360000
19 19156039 intron variant C/T snv 0.18
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs7360000
rs7360000
19 19156039 intron variant C/T snv 0.18
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs75746498
rs75746498
19 19149877 intron variant G/A;C;T snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018