Source: GWASDB

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: rs16853722
rs16853722
MECOM
3 169432844 intron variant T/C snv 0.11
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		0.800 1.000 1 2012 2012
dbSNP: rs448378
rs448378
MECOM
1.000 0.040 3 169383111 intron variant G/A;C snv
CUI: C0373675
Disease: Magnesium measurement
Magnesium measurement 		0.800 1.000 1 2010 2010
dbSNP: rs784288
rs784288
MECOM
1.000 0.080 3 169253443 intron variant A/G;T snv
CUI: C0029456
Disease: Osteoporosis
Osteoporosis 		0.800 1.000 1 2013 2013
dbSNP: rs6774494
rs6774494
MECOM
0.882 0.160 3 169364845 intron variant G/A snv 0.42
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.740 1.000 1 2010 2017
dbSNP: rs1343040
rs1343040
MECOM ; MECOM-AS1
3 169468505 intron variant G/A snv 0.36
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs1344555
rs1344555
MECOM
3 169582431 intron variant C/A;G;T snv
CUI: C3160731
Disease: Pulmonary function (finding)
Pulmonary function (finding) 		0.700 1.000 1 2011 2011
dbSNP: rs1344555
rs1344555
MECOM
3 169582431 intron variant C/A;G;T snv
CUI: C0231921
Disease: Pulmonary function
Pulmonary function 		0.700 1.000 1 2011 2011
dbSNP: rs16853540
rs16853540
MECOM
3 169343279 intron variant G/A snv 2.2E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs16853540
rs16853540
MECOM
3 169343279 intron variant G/A snv 2.2E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs16853540
rs16853540
MECOM
3 169343279 intron variant G/A snv 2.2E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1918974
rs1918974
MECOM ; MECOM-AS1
1.000 0.040 3 169448100 intron variant C/T snv 0.57
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2011 2011
dbSNP: rs1918974
rs1918974
MECOM ; MECOM-AS1
1.000 0.040 3 169448100 intron variant C/T snv 0.57
CUI: C1305849
Disease: Diastolic blood pressure measurement
Diastolic blood pressure measurement 		0.700 1.000 1 2009 2009
dbSNP: rs419076
rs419076
MECOM
3 169383098 intron variant T/A;C snv
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement 		0.700 1.000 1 2011 2011
dbSNP: rs419076
rs419076
MECOM
3 169383098 intron variant T/A;C snv
CUI: C1305849
Disease: Diastolic blood pressure measurement
Diastolic blood pressure measurement 		0.700 1.000 1 2011 2011
dbSNP: rs419076
rs419076
MECOM
3 169383098 intron variant T/A;C snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs448378
rs448378
MECOM
1.000 0.040 3 169383111 intron variant G/A;C snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2011 2011
dbSNP: rs448378
rs448378
MECOM
1.000 0.040 3 169383111 intron variant G/A;C snv
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement 		0.700 1.000 1 2009 2009
dbSNP: rs9290370
rs9290370
MECOM
3 169607225 intron variant T/G snv 0.78
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011