Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs35811052
rs35811052 		16 15034559 splice region variant A/G snv 0.25 0.24
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs3803573
rs3803573 		16 15044556 non coding transcript exon variant C/T snv 0.29
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.700 1.000 1 2019 2019
dbSNP: rs4122352
rs4122352 		16 15080714 intron variant G/A snv 0.21
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4985124
rs4985124 		16 15031584 intron variant T/G snv 0.30
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4985154
rs4985154 		16 15037785 3 prime UTR variant G/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4985155
rs4985155 		16 15035602 intron variant A/G snv 0.40 0.37
CUI: C0177804
Disease: Bone Mineral Density Test
Bone Mineral Density Test 		0.700 1.000 1 2012 2012
dbSNP: rs4985155
rs4985155 		16 15035602 intron variant A/G snv 0.40 0.37
CUI: C0562350
Disease: Hip circumference
Hip circumference 		0.700 1.000 1 2015 2015
dbSNP: rs4985155
rs4985155 		16 15035602 intron variant A/G snv 0.40 0.37
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4985167
rs4985167 		16 14989008 non coding transcript exon variant C/T snv 0.25
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs6498540
rs6498540 		16 15036737 3 prime UTR variant A/G snv 0.31
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7200543
rs7200543 		16 15036113 synonymous variant A/G snv 0.35 0.30
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs7200543
rs7200543 		16 15036113 synonymous variant A/G snv 0.35 0.30
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2017 2017
dbSNP: rs7200543
rs7200543 		16 15036113 synonymous variant A/G snv 0.35 0.30
CUI: C0337438
Disease: Glucose measurement
Glucose measurement 		0.700 1.000 1 2011 2011
dbSNP: rs7200543
rs7200543 		16 15036113 synonymous variant A/G snv 0.35 0.30
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		0.700 1.000 1 2011 2011
dbSNP: rs7200543
rs7200543 		16 15036113 synonymous variant A/G snv 0.35 0.30
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs8045034
rs8045034 		16 15027057 intron variant A/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs9888789
rs9888789 		16 15025034 intron variant C/A;G snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012