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: rs102275
rs102275
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 3 2011 2013
dbSNP: rs102275
rs102275
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs108499
rs108499
11 61779765 intron variant C/T snv 0.27
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs174528
rs174528
1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs174534
rs174534
1.000 0.080 11 61781986 non coding transcript exon variant A/G snv 0.28
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs174535
rs174535
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs174536
rs174536
11 61784455 non coding transcript exon variant A/C snv 0.29
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs174537
rs174537
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs174538
rs174538
0.701 0.440 11 61792609 5 prime UTR variant G/A snv 0.34 0.26
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs102274
rs102274
1.000 0.080 11 61790354 non coding transcript exon variant T/C snv 0.28
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs102275
rs102275
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.810 1.000 1 2010 2018
dbSNP: rs102275
rs102275
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs102275
rs102275
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47
High density lipoprotein measurement
0.800 1.000 1 2010 2012
dbSNP: rs102275
rs102275
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs102275
rs102275
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs102275
rs102275
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs102275
rs102275
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.800 1.000 1 2010 2010
dbSNP: rs102275
rs102275
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs108499
rs108499
11 61779765 intron variant C/T snv 0.27
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs149803
rs149803
11 61771548 synonymous variant C/G;T snv 0.18
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs149803
rs149803
11 61771548 synonymous variant C/G;T snv 0.18
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs149804
rs149804
11 61771134 intron variant A/G snv 0.31
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs174528
rs174528
1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs174529
rs174529
11 61776489 intron variant T/C snv 0.34
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs174530
rs174530
1.000 0.080 11 61779120 non coding transcript exon variant A/G snv 0.30
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012