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: rs17762454
rs17762454
0.925 0.120 6 7212967 non coding transcript exon variant C/T snv 0.25
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement
0.700 1.000 1 2012 2012
dbSNP: rs17762454
rs17762454
0.925 0.120 6 7212967 non coding transcript exon variant C/T snv 0.25
CUI: C1261430
Disease: Fasting blood sugar result
Fasting blood sugar result
0.700 1.000 1 2012 2012
dbSNP: rs2842895
rs2842895
0.925 0.120 6 7106083 upstream gene variant G/C snv 0.40
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.700 1.000 1 2013 2013
dbSNP: rs2842895
rs2842895
0.925 0.120 6 7106083 upstream gene variant G/C snv 0.40
CUI: C0018099
Disease: Gout
Gout
0.700 1.000 1 2013 2013
dbSNP: rs3778321
rs3778321
6 7250037 3 prime UTR variant G/A snv 0.11
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement
0.700 1.000 1 2012 2012
dbSNP: rs3778321
rs3778321
6 7250037 3 prime UTR variant G/A snv 0.11
CUI: C1261430
Disease: Fasting blood sugar result
Fasting blood sugar result
0.700 1.000 1 2012 2012
dbSNP: rs4585612
rs4585612
0.925 0.120 6 7152919 intron variant C/T snv 0.41
CUI: C0018099
Disease: Gout
Gout
0.700 1.000 1 2013 2013
dbSNP: rs4585612
rs4585612
0.925 0.120 6 7152919 intron variant C/T snv 0.41
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.700 1.000 1 2013 2013
dbSNP: rs557074
rs557074
1.000 0.040 6 7144958 intron variant T/G snv 0.27
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 1.000 1 2006 2006
dbSNP: rs6935691
rs6935691
6 7178306 intron variant T/A snv 0.28
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs9405328
rs9405328
6 7166005 intron variant A/G snv 0.29
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs9406002
rs9406002
6 7181502 non coding transcript exon variant A/G snv 0.25
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs9502560
rs9502560
6 7176907 intron variant T/G snv 0.29
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013
dbSNP: rs9505057
rs9505057
6 7171174 intron variant T/G snv 0.30
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2013 2013