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: rs11254363
rs11254363
CUBN
1.000 0.040 10 17088694 intron variant A/G snv 0.26
CUI: C0202252
Disease: VITAMIN B12 MEASUREMENT
VITAMIN B12 MEASUREMENT 		0.800 1.000 1 2009 2009
dbSNP: rs1801222
rs1801222
CUBN
0.925 0.160 10 17114152 missense variant A/G snv 0.73 0.72
CUI: C2242817
Disease: Homocysteine measurement
Homocysteine measurement 		0.800 1.000 1 2013 2013
dbSNP: rs1801222
rs1801222
CUBN
0.925 0.160 10 17114152 missense variant A/G snv 0.73 0.72
CUI: C0202252
Disease: VITAMIN B12 MEASUREMENT
VITAMIN B12 MEASUREMENT 		0.800 1.000 1 2009 2014
dbSNP: rs1801239
rs1801239
CUBN
0.827 0.160 10 16877053 missense variant T/C;G snv 8.9E-02; 8.0E-06
CUI: C0001925
Disease: Albuminuria
Albuminuria 		0.800 1.000 1 2011 2019
dbSNP: rs11254327
rs11254327
CUBN
10 17006709 intron variant C/T snv 0.40
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.700 1.000 1 2012 2012
dbSNP: rs12257093
rs12257093
CUBN
10 17022992 intron variant G/A snv 1.9E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12257093
rs12257093
CUBN
10 17022992 intron variant G/A snv 1.9E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs17139292
rs17139292
CUBN
10 16828081 intron variant G/A snv 1.9E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs17139292
rs17139292
CUBN
10 16828081 intron variant G/A snv 1.9E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs17139292
rs17139292
CUBN
10 16828081 intron variant G/A snv 1.9E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1891473
rs1891473
CUBN
10 16861081 intron variant T/C snv 0.19
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1891473
rs1891473
CUBN
10 16861081 intron variant T/C snv 0.19
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7898873
rs7898873
CUBN
10 16835081 missense variant G/A;C snv 4.0E-06; 1.8E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7898873
rs7898873
CUBN
10 16835081 missense variant G/A;C snv 4.0E-06; 1.8E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7921488
rs7921488
CUBN
1.000 0.080 10 17127078 intron variant A/G snv 0.90
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 1.000 1 2014 2014