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: rs2714337
rs2714337
6 7240344 intron variant A/T snv 0.34
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 1.000 1 2012 2012
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: rs6931262
rs6931262
6 7217284 non coding transcript exon variant C/T snv 0.10
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.800 1.000 1 2013 2013
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
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: rs1285875
rs1285875
0.925 0.120 6 7115694 intron variant G/A;C snv 0.63
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.700 1.000 2 2010 2013
dbSNP: rs1285875
rs1285875
0.925 0.120 6 7115694 intron variant G/A;C snv 0.63
CUI: C0018099
Disease: Gout
Gout
0.700 1.000 2 2010 2013
dbSNP: rs1285879
rs1285879
0.925 0.120 6 7137130 intron variant T/C snv 0.67
CUI: C0018099
Disease: Gout
Gout
0.700 1.000 2 2010 2013
dbSNP: rs1285879
rs1285879
0.925 0.120 6 7137130 intron variant T/C snv 0.67
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.700 1.000 2 2010 2013
dbSNP: rs1334577
rs1334577
0.925 0.120 6 7211518 intron variant G/A snv 0.23
CUI: C0018099
Disease: Gout
Gout
0.700 1.000 2 2010 2013
dbSNP: rs1334577
rs1334577
0.925 0.120 6 7211518 intron variant G/A snv 0.23
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.700 1.000 2 2010 2013
dbSNP: rs622404
rs622404
0.925 0.120 6 7130363 intron variant A/G snv 0.68
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.700 1.000 2 2010 2013
dbSNP: rs622404
rs622404
0.925 0.120 6 7130363 intron variant A/G snv 0.68
CUI: C0018099
Disease: Gout
Gout
0.700 1.000 2 2010 2013
dbSNP: rs630258
rs630258
0.925 0.120 6 7134168 intron variant T/C snv 0.67
CUI: C0018099
Disease: Gout
Gout
0.700 1.000 2 2010 2013
dbSNP: rs630258
rs630258
0.925 0.120 6 7134168 intron variant T/C snv 0.67
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.700 1.000 2 2010 2013
dbSNP: rs665723
rs665723
0.925 0.120 6 7138831 intron variant C/T snv 0.67
CUI: C0018099
Disease: Gout
Gout
0.700 1.000 2 2010 2013
dbSNP: rs665723
rs665723
0.925 0.120 6 7138831 intron variant C/T snv 0.67
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.700 1.000 2 2010 2013
dbSNP: rs687467
rs687467
0.925 0.120 6 7127843 intron variant A/G;T snv
CUI: C0018099
Disease: Gout
Gout
0.700 1.000 2 2010 2013
dbSNP: rs687467
rs687467
0.925 0.120 6 7127843 intron variant A/G;T snv
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.700 1.000 2 2010 2013
dbSNP: rs6933716
rs6933716
0.925 0.120 6 7125476 intron variant T/C snv 0.53
CUI: C0018099
Disease: Gout
Gout
0.700 1.000 2 2010 2013